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Journal articles on the topic 'Ichthyosis vulgaris'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Traupe, Heiko, and Vinzenz Oji. "Neue Erkenntnisse zum Thema Ichthyose." Kinder- und Jugendmedizin 7, no. 05 (2007): 247–56. http://dx.doi.org/10.1055/s-0038-1625673.

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ZusammenfassungIchthyosen umfassen eine ätiologisch heterogene Gruppe von Verhornungsstörungen, die die gesamte Haut betreffen und durch sichtbare Schuppung und Verdickung der Hornhaut charakterisiert sind. Häufig besteht zusätzlich ein Erythem. Neben der Unterteilung in kongenital und nicht-kongenital unterscheidet man isolierte Ichthyosen, wie die X-chromosomal rezessive Ichthyose oder lamelläre Ichthyose, von Ichthyose-Syndromen, wie das Comèl-Netherton- oder Sjögren-Larsson-Syndrom. Kongenitale Ichthyosen sind selten und manifestieren sich unter dem Bild eines Kollodiumbabys oder als kongenitale ichthyosiforme Erythrodermie. In den letzten Jahren wurden erneut wichtige Meilensteine der Ichthyoseforschung passiert, z. B. die molekulargenetische Aufklärung der Harlekin-Ichthyose und Ichthyosis vulgaris. Trotz meist fehlender kausaler Therapiemöglichkeit stellt die verbesserte Diagnostik einen großen Gewinn für Betroffene dar. Darüber hinaus existieren mannigfache symptomatische Therapieoptionen. Hilfreiche Organisationen in Deutschland stellen die Selbsthilfe Ichthyose e. V. (www.ichthyose.de) und das Netzwerk für Ichthyose und verwandte Verhornungsstörungen (NIRK) (www.netzwerk-ichthyose.de) dar.

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2

Hassan, Md Kamrul, Aloke Kumar Saha, Poly Begum, Tahmina Akter, and Shyamol Kumar Saha. "A Case Report on Congenital Ichthyosis - Collodion Baby." Faridpur Medical College Journal 11, no. 1 (December 29, 2016): 39–42. http://dx.doi.org/10.3329/fmcj.v11i1.30880.

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Collodion baby describes a highly characteristic clinical entity in newborns encased in a yellowish translucent membrane resembling collodion. In most cases the condition either precedes the development of one of a variety of ichthyoses, the commonest of which are lamellar ichthyosis and non-bullous ichthyosiform erythroderma, or occasionally represents an initial phase of other ichthyoses such as ichthyosis vulgaris. In at least 10% of all cases of collodion baby, the condition is followed by a mild ichthyosis of lamellar type, so mild as to be considered more or less normal, so-called self-healing collodion baby or 'lamellar ichthyosis of the newborn'. In this report, we present a severe form of ichthyosis.Faridpur Med. Coll. J. Jan 2016;11(1): 39-42

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3

Stojanović, Vesna, Aleksandra Doronjski, Slobodan Spasojević, Nataša Stašuk, and Anica Radulović. "Collodion Baby - a Case Report." Serbian Journal of Dermatology and Venereology 6, no. 4 (December 1, 2014): 186–90. http://dx.doi.org/10.2478/sjdv-2014-0016.

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Abstract Colloidon baby describes a highly characteristic clinical entity in newborns encased in a yellowish translucent membrane resembling collodion. In most cases the condition either precedes the development of one of a variety of ichthyoses, the commonest of which are lamellar ichthyosis and non-bullous ichthyosiform erythroderma, or occasionally represents an initial phase of other ichthyoses such as ichthyosis vulgaris. In at least 10% of all cases of collodion baby, the condition is followed by a mild ichthyosis of lamellar type, so mild as to be considered more or less normal, so-called self-healing collodion baby or ‘lamellar ichthyosis of the newborn’. In this report we present a rare case of collodion baby in whom, after collodion membrane peeled-off, the skin retained normal appearance.

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4

Fitch, Naomi. "Ichthyosis vulgaris." Clinical Genetics 15, no. 2 (April 23, 2008): 206. http://dx.doi.org/10.1111/j.1399-0004.1979.tb01766.x.

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5

Fitch, Dr Naomi. "Dominant ichthyosis vulgaris." Clinical Genetics 11, no. 3 (April 23, 2008): 311–12. http://dx.doi.org/10.1111/j.1399-0004.1977.tb01318.x.

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6

Fozia, Fozia, Rubina Nazli, Sher Alam Khan, Ahmed Bari, Abdul Nasir, Riaz Ullah, Hafiz Majid Mahmood, et al. "Novel Homozygous Mutations in the Genes TGM1, SULT2B1, SPINK5 and FLG in Four Families Underlying Congenital Ichthyosis." Genes 12, no. 3 (March 5, 2021): 373. http://dx.doi.org/10.3390/genes12030373.

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Background: Ichthyoses are a large group of hereditary cornification disorders, which are both clinically and etiologically heterogeneous and affect mostly all the skin surface of the patients. Ichthyosis has its origin in an ancient Greek word “ichthys” meaning fish, this is because the ichthyosis patients have dry, thickened, and scaly skin. There is an excess accumulation of epidermal cells resulting in the appearance of continuous and widespread scales on the body. There are many varieties of ichthyosis with a broad spectrum of intensity, severity, and associated symptoms, most of them are extremely rare. Ichthyosis vulgaris is the most frequently occurring type of ichthyoses. Method: The present study consists of four Pakistani ichthyosis families (A, B, C, and D). Whole exome sequencing (WES) approach was used to identify the pathogenic sequence variants in probands. The segregation of these variants in other participants was confirmed by Sanger sequencing. Results: Total four variants including, two splice site (TGM1: c.2088 + 1G > A) and (SPINK5: c.882 + 1G > T), a missense (SULT2B1: c.419C > T; p. Ala140Val), and a nonsense (FLG: c.6109C > T; p. Arg2037Ter) variant were identified in families A, C, B, and D, respectively, as causative mutations responsible for ichthyosis in these families. Conclusion: Our study unravels the molecular etiology of the four Pakistani ichthyosis families and validates the involvement of TGM1, SULT2B1, SPINK5, and FLG, in the etiology of different forms of ichthyosis. In addition, this study also aims to give a detailed clinical report of the studied ichthyosis families.

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7

Oji, Vinzenz. "Ichthyosis vulgaris von X-chromosomal rezessiver Ichthyose unterscheiden." hautnah dermatologie 33, no. 5 (September 2017): 40–43. http://dx.doi.org/10.1007/s15012-017-2523-6.

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8

Oji, Vinzenz. "Ichthyosis vulgaris von X-chromosomal rezessiver Ichthyose unterscheiden." pädiatrie: Kinder- und Jugendmedizin hautnah 27, S7 (August 2015): 6–10. http://dx.doi.org/10.1007/s15014-015-0454-4.

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9

Fedota, O. M., Yu O. Sadovnychenko, L. V. Roshchenyuk, V. M. Vorontsov, and P. P. Ryzhko. "Study of prevalence of different forms of ichthyosis in Kharkiv region." Faktori eksperimental'noi evolucii organizmiv 23 (September 9, 2018): 244–48. http://dx.doi.org/10.7124/feeo.v23.1022.

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Ichthyosis is genetically and clinically heterogenic group of epidermis keratinization disorders. Its prevalence is geographically different. Aim. The aim of this research was to evaluate ichthyosis prevalence in Kharkiv region. Methods. The collection of clinical-genealogical history was carried out by the method of single registration of the proband on the basis of the Regional Clinical Dermatological and Venereological Health Center No. 1 and the Dermatovenerological Health Centers of the Kharkiv Region in 2017. Results. The ichthyosis prevalence in Kharkiv region was 2.5·10–4 in 2017. The ichthyosis prevalence varied from 6.7∙10‑5 in Krasnohrad district to 1.0∙10‑3 in Dvorichna district. The least prevalence was in the population of Vovchansk city (1.1∙10‑4) and the highest one was in the population of Dvorichna city (10.7∙10‑4). The differences between the prevalence of ichthyosis vulgaris in Kharkiv region in 2008-2017 were established. Conclusions. It was found that the decrease of ichthyosis prevalence in Kharkiv region was 1.6 times during last 10 years. This index for ichthyosis vulgaris was decreased 1.9 times at the same period. Monogenic dermatoses, as an example of ichthyosis, can be used both to monitor the burden of genetic disorders in the region and to solve the problems of general and personal genetic safety in the population. Keywords: ichthyosis vulgaris, X-linked recessive ichthyosis, prevalence.

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10

Rabinowitz, L. G., and N. B. Esterly. "Atopic Dermititis and Ichthyosis Vulgaris." Pediatrics in Review 15, no. 6 (June 1, 1994): 220–26. http://dx.doi.org/10.1542/pir.15-6-220.

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11

Okulicz, Jason F., and Robert A. Schwartz. "Hereditary and acquired ichthyosis vulgaris." International Journal of Dermatology 42, no. 2 (February 2003): 95–98. http://dx.doi.org/10.1046/j.1365-4362.2003.01308.x.

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12

Agostini, G., V. Geti, Elisa M. Difonzo, and B. Giannotti. "Dermatophyte infection in ichthyosis vulgaris*." Mycoses 35, no. 7-8 (April 24, 2009): 197–99. http://dx.doi.org/10.1111/j.1439-0507.1992.tb00846.x.

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13

Fedota, Olena, Iurii Sadovnychenko, Lilia Chorna, Larysa Roshcheniuk, Vitalii Vorontsov, Pavlo Ryzhko, Ivanna Haybonyuk, Serhii Belyaev, Igor Belozorov, and Halyna Makukh. "The Effects of Polymorphisms in One-carbon Metabolism Genes on Manifestation of Ichthyosis Vulgaris." Open Access Macedonian Journal of Medical Sciences 9, A (May 14, 2021): 291–97. http://dx.doi.org/10.3889/oamjms.2021.6004.

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BACKGROUND: Ichthyosis vulgaris is the most common type of Mendelian disorders of cornification, caused by loss-of-function mutations in the gene encoding epidermal protein filaggrin (FLG), namely R501X and 2282del4. FLG 2282del4 mutation in heterozygotes is incompletely penetrant. Polymorphisms in one-carbon metabolism genes could be associated with clinical manifestation of ichthyosis vulgaris. AIM: The purpose of the present study was to analyze the effects of MTHFR, MTR and MTRR polymorphisms in patients with ichthyosis vulgaris. METHODS: 31 patients with ichthyosis vulgaris, 7 their FLG heterozygous relatives without symptoms of disorder, and 150 healthy controls were enrolled in study. FLG null mutations —R501X (rs61816761) and 2282del4 (rs558269137) — and one-carbon metabolism gene polymorphisms — MTHFR C677T (rs1801133), MTHFR A1298C (rs1801131), MTR A2756G (rs1805087) and MTRR A66G (rs1801394) — were analyzed by a polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) assay. RESULTS: Among patients with ichthyosis, heterozygous for FLG 2282del4 mutation, the distributions of genotypes for folate metabolism genes were: MTHFR C677T CC:CT:TT —29.4%:70.6%:0.0%; MTHFR A1298C AA:AC:CC — 52.9%:47.1%:0.0%; MTR A2756G AA:AG:GG — 70.3%:23.5%:5.9%; MTRR A66G AA:AG:GG — 23.4%:52.9%:23.5%. The frequencies of MTR 2756AA and MTRR 66GG genotypes were 1.4–1.6 times higher in affected individuals heterozygous for 2282del4 than in patients with other FLG genotypes. In affected 2282del4 heterozygotes, the frequency of MTR 2756AA genotype was 1.6 times greater than in healthy controls (p<0.01). The strongest association was found between MTHFR 677CT/MTHFR 1298AA/MTR 2756AA/MTRR 66AG genotype and ichthyosis — OR=11.23 (95% CI 2.51−50.21, p=0.002). CONCLUSIONS: Various genotypes of one-carbon metabolism genes increase the risk of ichthyosis in heterozygotes for the FLG 2282del4 mutation (OR 2.799‑11.231). The most probable predisposing genotype is 677CT/1298AA/2756AA+AG/66AG.

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14

Xu, Xinxin, Qingqing Ma, Mu Lin, Mubo Liu, Chaolin Huang, Jianchao Ying, and Jun Ye. "A loss of function mutation in the filaggrin gene associated with ichthyosis vulgaris and rheumatoid arthritis." European Journal of Inflammation 19 (January 2021): 205873922110328. http://dx.doi.org/10.1177/20587392211032805.

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Introduction Mutations in the filaggrin ( FLG) gene are known to cause ichthyosis vulgaris. Methods We used whole-genome sequencing (WGS) technology to investigate the genetic causes of rare and complex inherited diseases including rheumatoid arthritis, ichthyosis, and congenital fibrosis of the extraocular muscles type 1 (CFEOM1) in a Chinese family. WGS was performed in four topics, and the identified candidate mutations were further verified through Sanger sequencing. Results We identified a mutation in FLG gene (g.152280098 C>A, p.E2422∗) that may be associated with ichthyosis and arthritis. Moreover, a mutation in KIF21A (g.39726207 G>A, p.R954 W) was also determined in affected members as the cause of CFEOM1. The gene interaction network demonstrated an interesting correlation between FLG and genes associated with arthritis and ichthyosis. Functional enrichment analysis of these interacting genes revealed several possible pathways that might be linked to arthritis and ichthyosis. Conclusion In general, we confirmed a loss of function mutation in the FLG gene associated with ichthyosis vulgaris and rheumatoid arthritis in this family.

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15

Nopriyati, Deddy Deddy, Rusmawardiana, and Mutia Devi. "Epidermal Proliferation and Differentiation in Ichthyosis Vulgaris." Bioscientia Medicina : Journal of Biomedicine and Translational Research 5, no. 2 (January 19, 2021): 266–78. http://dx.doi.org/10.32539/bsm.v5i2.214.

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A B S T R A C TEpidermal proliferation and differentiation is a physiological process which playscrucial role in protecting human body from external environment. Ichthyosisvulgaris is a disease caused by disruption of epidermal differentiation process.Disrupted of profilaggrin conversion to filaggrin caused by mutations from thefilaggrin gene (FLG) located on chromosome 1q21. Recently, caused of ichthyosisvulgaris is mutation of the CASP14 gene on chromosome 19p13.12 which producescaspase-14, is involved in the proteolytic degradation of filaggrin. Clinicalmanifestations of ichthyosis vulgaris are hyperlinear palmar and plantar, keratosispilaris, xerosis, and localized or generalized scaling of the skin. Application ofemollients, humectants and keratolytic agents are the main treatment of ichthyosisvulgaris. Further research on caspase-14 as a therapeutic target is needed in thetreatment of ichthyosis vulgaris.

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16

Thyssen, J. P., E. Godoy-Gijon, and P. M. Elias. "Ichthyosis vulgaris: the filaggrin mutation disease." British Journal of Dermatology 168, no. 6 (May 6, 2013): 1155–66. http://dx.doi.org/10.1111/bjd.12219.

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17

A. Cuevas-Covarrubias, M. Valdes-Fl, S. "Ichthyosis Vulgaris and X-linked Ichthyosis: Simultaneous Segregation in the Same Family." Acta Dermato-Venereologica 79, no. 6 (October 20, 1999): 494–95. http://dx.doi.org/10.1080/000155599750010120.

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18

Kshirsagar, Vinayak. "Ichthyosis vulgaris and pycnodysostosis: an unusual occurrence." Acta Medica Academica 41, no. 2 (November 27, 2012): 214–18. http://dx.doi.org/10.5644/ama2006-124.54.

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19

Reißer, Ch, H. Enzmann, S. Günzel, I. Anton-Lamprecht, and I. A. Born. "Ozaena und allergische Rhinitis bei Ichthyosis vulgaris*." Laryngo-Rhino-Otologie 71, no. 06 (June 1992): 302–6. http://dx.doi.org/10.1055/s-2007-997300.

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20

ELSAYED-ALI, H., S. BARTON, and R. MARKS. "Stereological studies of desmosomes in ichthyosis vulgaris." British Journal of Dermatology 126, no. 1 (January 1992): 24–28. http://dx.doi.org/10.1111/j.1365-2133.1992.tb08398.x.

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21

Kim, Eun Joo, Mi Sook Jeong, Kapsok Li, Mi Kyung Park, Mi-Kyung Lee, Yoosik Yoon, Dae-Yeon Cho, and Seong Jun Seo. "Genetic Polymorphism ofFLGin Korean Ichthyosis Vulgaris Patients." Annals of Dermatology 23, no. 2 (2011): 170. http://dx.doi.org/10.5021/ad.2011.23.2.170.

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22

Tas, Faruk, Kayhan Erturk, Cuyan Demirkesen, and Fatih Goktay. "Cutaneous Melanoma in Association With Ichthyosis Vulgaris." Journal of Pediatric Hematology/Oncology 39, no. 8 (November 2017): 630. http://dx.doi.org/10.1097/mph.0000000000000953.

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23

Goksu, Yasemin Azize, Oner Ozdemir, Ercan Tunc, and Mehmet Sahin. "F.71. CVID and Acquired Ichthyosis Vulgaris." Clinical Immunology 127 (January 2008): S66—S67. http://dx.doi.org/10.1016/j.clim.2008.03.183.

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24

Lai-Cheong, Joey E., and John A. McGrath. "Advances in understanding the genetic basis of inherited single gene skin barrier disorders: new clues to key genes that may be involved in the pathogenesis of atopic dermatitis." Anais Brasileiros de Dermatologia 81, no. 6 (December 2006): 567–71. http://dx.doi.org/10.1590/s0365-05962006000600009.

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Increasing knowledge of genomic DNA sequences and genetic databases has led to the characterization of the molecular basis of several inherited skin disorders. In this review we summarize some of the major recent discoveries that have been made in defining the pathogenic mutations that cause inherited disorders of the skin barrier leading to skin scaling or increased transepidermal water loss in either rare disorders (Netherton’s syndrome or harlequin ichthyosis) or more common genodermatoses (ichthyosis vulgaris). These molecular breakthroughs have led to more accurate diagnoses, better genetic counselling and, where appropriate, the feasibility of DNA-based prenatal diagnosis, as well as the possibility of developing newer forms of treatment, including gene or protein therapy. Identifying the molecular basis of these conditions, especially ichthyosis vulgaris, has also provided dramatic new insight into the genetic abnormalities in the common disorder, atopic dermatitis. Thus research on the relatively rare single gene inherited skin disorders not only has benefits for patients and their families with these uncommon conditions but also has the potential to yield fresh and significant new information about very common skin diseases.

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25

Anton-Lamprecht, I., and U. W. Schnyder. "Ultrastructural distinct ion of autosomal dominant ichthyosis vulgaris and X-linked recessive ichthyosis." Clinical Genetics 10, no. 4 (April 23, 2008): 245–47. http://dx.doi.org/10.1111/j.1399-0004.1976.tb00044.x.

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26

Nima-Zegarra, Harry, Ray Shepherd, and Samira Shojaee. "Diffuse Tracheobronchial Inflammation and Stenosis in Ichthyosis Vulgaris." Chest 144, no. 4 (October 2013): 31A. http://dx.doi.org/10.1378/chest.1703126.

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27

Abd-Rabbo, Fatma A., Rania A. El-Tatawy, Omnia M. K. Rizk, and Mona M. Elshalaby. "Filaggrin expression in atopic dermatitis and ichthyosis vulgaris." Egyptian Journal of Pathology 34, no. 2 (December 2014): 130–35. http://dx.doi.org/10.1097/01.xej.0000455926.49150.9e.

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28

Errichetti, E., G. Stinco, E. Pegolo, and P. Patrone. "Acquired ichthyosis during acitretin therapy for psoriasis vulgaris." Journal of the European Academy of Dermatology and Venereology 30, no. 1 (August 29, 2014): 181–82. http://dx.doi.org/10.1111/jdv.12690.

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29

Hernández-Martin, Angela, Beatriz Aranegui, Ana Martin-Santiago, and Ignacio Garcia-Doval. "A systematic review of clinical trials of treatments for the congenital ichthyoses, excluding ichthyosis vulgaris." Journal of the American Academy of Dermatology 69, no. 4 (October 2013): 544–49. http://dx.doi.org/10.1016/j.jaad.2013.05.017.

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30

Живайкина, Н. А., Е. В. Малютина, Д. А. Машкевич, М. А. Васильева, and Ю. В. Максимова. "Mutation variability in the filaggrin gene in patients with ichthyosis vulgaris." Nauchno-prakticheskii zhurnal «Medicinskaia genetika», no. 8(217) (August 31, 2020): 105–6. http://dx.doi.org/10.25557/2073-7998.2020.08.105-106.

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Обследован 21 пациент с клиническими проявлениями вульгарного ихтиоза. Наиболее часто у них выявлялась мутация 2282del4 в гене FLG как в гомозиготном (у 6 больных), так и в гетерозиготном состояниях. We examined 21 patients with clinical manifestations of ichthyosis vulgaris. Most often, they had the 2282del4 mutation in the FLG gene both in homozygous (in 6 patients) and heterozygous states.

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31

OKANO, M., Y. KITANO, K. YOSHIKAWA, T. NAKAMURA, Y. MATSUZAWA, and T. YUASA. "X-linked ichthyosis and ichthyosis vulgaris: comparison of their clinical features based on biochemical analysis." British Journal of Dermatology 119, no. 6 (December 1988): 777–83. http://dx.doi.org/10.1111/j.1365-2133.1988.tb03503.x.

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32

YOSHIIKE, T., T. MATSUI, and H. OGAWA. "Steroid sulphatase deficiency in patients initially diagnosed as ichthyosis vulgaris or recessive X-linked ichthyosis." British Journal of Dermatology 112, no. 4 (April 1985): 431–33. http://dx.doi.org/10.1111/j.1365-2133.1985.tb02316.x.

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33

Ibi, Naotaka, Yoshihira Fukuoka, Takao Hotokebuchi, Seiya Jingushi, Yukihiro Kai, Kunimasu Ohya, Yoshio Tamechika, Tsuyoshi Inoue, and Masaaki Mezuki. "Osteopoikilosis associated with both ichthyosis vulgaris and Crohn's disease." Orthopedics & Traumatology 33, no. 4 (1985): 1204–8. http://dx.doi.org/10.5035/nishiseisai.33.1204.

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34

Fedota, O. M., L. V. Roshcheniuk, V. M. Vorontsov, O. S. Solodyankin, I. A. Sadovnychenko, and J. V. Gontar. "Polymorphism of FLG Gene in Patients with Ichthyosis Vulgaris." Ukraïnsʹkij žurnal medicini, bìologìï ta sportu 1, no. 1 (March 10, 2016): 185–88. http://dx.doi.org/10.26693/jmbs01.01.185.

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35

Mondal, Surojit. "Monostotic Fibrous Dysplasia and Ichthyosis Vulgaris ------ A Rare Association." IOSR Journal of Dental and Medical Sciences 5, no. 1 (2013): 4–7. http://dx.doi.org/10.9790/0853-0510407.

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36

Compton, John G., John J. DiGiovanna, Regina Bailey, Frances Austin, Phillip Fleckman, and Sherri J. Bale. "In pursuit of the molecular basis of ichthyosis vulgaris." Journal of Dermatological Science 16 (March 1998): S147. http://dx.doi.org/10.1016/s0923-1811(98)83879-6.

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37

Saatci, A. Osman, Zeynep Özbek, Süheyla Köse, Ismet Durak, and Salih Kavukçu. "An unusual central retinal dystrophy associated with ichthyosis vulgaris." Ophthalmic Genetics 21, no. 2 (January 2000): 101–7. http://dx.doi.org/10.1076/1381-6810(200006)2121-8ft101.

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38

Saatci, A. Osman, Zeynep �zbek, S�heyla K�se, Ismet Durak, and Salih Kavuk�u. "An unusual central retinal dystrophy associated with ichthyosis vulgaris." Ophthalmic Genetics 21, no. 2 (June 1, 2000): 101–7. http://dx.doi.org/10.1076/1381-6810(200006)21:2;1-8;ft101.

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39

Fitch, Naomi, Richard Segool, Alex Ferenczy, and Howard Cohen. "Dominant ichthyosis vulgaris with an ultrastructuraally normal granular layer." Clinical Genetics 9, no. 1 (April 23, 2008): 71–76. http://dx.doi.org/10.1111/j.1399-0004.1976.tb01551.x.

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40

Fartasch, Manigé, Thomas L. Diepgen, and Otto Paul Hornstein. "Atopic Dermatitis – Ichthyosis vulgaris – Hyperlinear Palms – an Ultrastructural Study." Dermatology 178, no. 4 (1989): 202–5. http://dx.doi.org/10.1159/000248427.

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41

Wang, Fusheng, Man Mao-Qiang, and Peter M. Elias. "A lipid mixture improves skin hydration in ichthyosis vulgaris." International Journal of Dermatology 36, no. 11 (June 28, 2008): 876–77. http://dx.doi.org/10.1111/j.1365-4362.1997.tb04142.x.

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42

BOGGIO, PAULA, MARIA CECÍLIA DA M. R. MACHADO, ZILDA N. P. DE OLIVEIRA, and MIRIAN N. SOTTO. "Methylmalonic Acidemia Presenting with an Ichthyosis Vulgaris-like Aspect." Pediatric Dermatology 24, no. 4 (July 2007): 455–56. http://dx.doi.org/10.1111/j.1525-1470.2007.00486.x.

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Gruber, Robert, Andreas R. Janecke, Christine Fauth, Gerd Utermann, Peter O. Fritsch, and Matthias Schmuth. "Filaggrin mutations p.R501X and c.2282del4 in ichthyosis vulgaris." European Journal of Human Genetics 15, no. 2 (December 13, 2006): 179–84. http://dx.doi.org/10.1038/sj.ejhg.5201742.

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Hoetzenecker, W., S. Schanz, M. Schaller, and G. Fierlbeck. "Generalized tinea corporis due to Trichophyton rubrum in ichthyosis vulgaris." Journal of the European Academy of Dermatology and Venereology 21, no. 8 (September 2007): 1129–31. http://dx.doi.org/10.1111/j.1468-3083.2006.02117.x.

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McClymont, L. F., and M. Ng. "A unique case of a digital tourniquet in ichthyosis vulgaris." JPRAS Open 23 (March 2020): 37–49. http://dx.doi.org/10.1016/j.jpra.2019.09.001.

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Fleckman, Philip, Karen A. Holbrook, Beverly A. Dale, and Virginia P. Sybert. "Keratinocytes Cultured From Subjects With Ichthyosis Vulgaris Are Phenotypically Abnormal." Journal of Investigative Dermatology 88, no. 5 (May 1987): 640–45. http://dx.doi.org/10.1111/1523-1747.ep12470251.

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McLean, W. H. I. "Filaggrin failure - from ichthyosis vulgaris to atopic eczema and beyond." British Journal of Dermatology 175 (September 26, 2016): 4–7. http://dx.doi.org/10.1111/bjd.14997.

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Lundborg, H. "Geschlechtsgebundene Vererbung von Ichthyosis Simplex (Vulgaris) in Einer Schwedischen Bauernsippe." Hereditas 9, no. 1-3 (July 9, 2010): 45–48. http://dx.doi.org/10.1111/j.1601-5223.1927.tb03507.x.

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Zhong, Wei, Bin Cui, Yizhi Zhang, Haisong Jiang, Shengcai Wei, Lei Bu, Guoping Zhao, Landian Hu, and Xiangyin Kong. "Linkage analysis suggests a locus of ichthyosis vulgaris on 1q22." Journal of Human Genetics 48, no. 7 (June 28, 2003): 390–92. http://dx.doi.org/10.1007/s10038-003-0043-1.

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Germann, Roger, Ingo Schindera, Matthias Kuch, Udo Seitz, Stefan Altmeyer, and Frank Schindera. "Lebensbedrohliche Salicylatintoxikation durch perkutane Resorption bei einer schweren Ichthyosis vulgaris." Der Hautarzt 47, no. 8 (August 15, 1996): 624–27. http://dx.doi.org/10.1007/s001050050479.

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