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Artykuły w czasopismach na temat „Keratosis Pilaris Atrophicans”

Autor: Grafiati
Data publikacji: 3 czerwca 2025
Data aktualizacji: 31 lipca 2025

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Sprawdź 28 najlepszych artykułów w czasopismach naukowych na temat „Keratosis Pilaris Atrophicans”.

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1

Oranje, Arnold P. "Keratosis Pilaris Atrophicans." Archives of Dermatology 130, no. 4 (1994): 500. http://dx.doi.org/10.1001/archderm.1994.01690040104017.

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Arnold, Andreas W., and Stanislaw A. Buechner. "Keratosis pilaris and keratosis pilaris atrophicans faciei." JDDG 4, no. 4 (2006): 319–23. http://dx.doi.org/10.1111/j.1610-0387.2006.05933.x.

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Arnold, Andreas W., and Stanislaw A. Buechner. "Keratosis pilaris und Keratosis pilaris atrophicans faciei." JDDG 4, no. 4 (2006): ———. http://dx.doi.org/10.1111/j.1610-0387.2006.05933suppl.x.

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4

DRAGO, F., G. MAIETTA, A. PARODI, and A. REBORA. "Keratosis pilaris decalvans non-atrophicans." Clinical and Experimental Dermatology 18, no. 1 (1993): 45–46. http://dx.doi.org/10.1111/j.1365-2230.1993.tb00965.x.

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5

Khumalo, NP, WJ Loo, K. Hollowood, I. Salvary, RM Graham, and RPR Dawber. "Keratosis pilaris atrophicans in mother and daughter." Journal of the European Academy of Dermatology and Venereology 16, no. 4 (2002): 397–400. http://dx.doi.org/10.1046/j.1468-3083.2002.00472.x.

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6

Callaway, Sanders R., and Jack L. Lesher. "Keratosis Pilaris Atrophicans: Case Series and Review." Pediatric Dermatology 21, no. 1 (2004): 14–17. http://dx.doi.org/10.1111/j.0736-8046.2004.21103.x.

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7

Miranda, B. H., N. Farjo, and B. Farjo. "Eyebrow reconstruction in dormant keratosis pilaris atrophicans." Journal of Plastic, Reconstructive & Aesthetic Surgery 64, no. 12 (2011): e303-e305. http://dx.doi.org/10.1016/j.bjps.2011.06.009.

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8

Dajani, Zeina A. W., Mary Jo Kerns, and Diya F. Mutasim. "Unilateral keratosis pilaris atrophicans faciei mimicking follicular mucinosis." Journal of the American Academy of Dermatology 64, no. 5 (2011): e71-e72. http://dx.doi.org/10.1016/j.jaad.2010.03.024.

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9

Cohen-Barak, E., N. Danial-Farran, H. Hammad, et al. "Desmoglein 4 Mutation Underlies Autosomal Recessive Keratosis Pilaris Atrophicans." Acta Dermato Venereologica 98, no. 8 (2018): 809–10. http://dx.doi.org/10.2340/00015555-2976.

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10

Alcántara González, J., P. Boixeda, MT Truchuelo Díez, and B. Fleta Asín. "Keratosis pilaris rubra and keratosis pilaris atrophicans faciei treated with pulsed dye laser: report of 10 cases." Journal of the European Academy of Dermatology and Venereology 25, no. 6 (2010): 710–14. http://dx.doi.org/10.1111/j.1468-3083.2010.03772.x.

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11

Tanghetti, E. A. "Keratosis pilaris rubra and keratosis pilaris atrophicans faciei treated with pulsed dye laser: report of 10 cases." Yearbook of Dermatology and Dermatologic Surgery 2012 (January 2012): 464–65. http://dx.doi.org/10.1016/j.yder.2011.11.039.

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12

McHenry, P. M., N. C. Nevin, and E. A. Bingham. "The Association of Keratosis Pilaris Atrophicans with Hereditary Woolly Hair." Pediatric Dermatology 7, no. 3 (1990): 202–4. http://dx.doi.org/10.1111/j.1525-1470.1990.tb00283.x.

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13

Rodríguez-Lojo, Romina, Jesus Del Pozo, Juan Manuel Barja, Francisca Piñeyro, and Lucia Pérez-Varela. "Keratosis pilaris atrophicans: Treatment with intense pulsed light in four patients." Journal of Cosmetic and Laser Therapy 12, no. 4 (2010): 188–90. http://dx.doi.org/10.3109/14764172.2010.502456.

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14

Clark, S. M., C. M. Mills, and S. W. Lanigan. "Treatment of keratosis pilaris atrophicans with the pulsed tunable dye laser." Journal of Cutaneous Laser Therapy 2, no. 3 (2000): 151–56. http://dx.doi.org/10.1080/14628830050516416.

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15

Di Lernia, Vito, and Cinzia Ricci. "Folliculitis Spinulosa Decalvans: An Uncommon Entity within the Keratosis Pilaris Atrophicans Spectrum." Pediatric Dermatology 23, no. 3 (2006): 255–58. http://dx.doi.org/10.1111/j.1525-1470.2006.00229.x.

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16

Stojanović, Slobodan, Nada Vučković, and Marina Jovanović. "Overlap Between Ulerythema Ophryogenes and Keratosis Follicularis Spinulosa Decalvans: a Case Report." Serbian Journal of Dermatology and Venereology 7, no. 3 (2015): 129–38. http://dx.doi.org/10.1515/sjdv-2015-0012.

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Abstract Ulerythema ophryogenes and keratosis follicularis spinulosa decalvans are rare folliculocentric keratotic disorders, from the group of follicular genokeratoses, characterized by keratosis pilaris atrophicans: follicular keratotic papules, sometimes with surrounding erythema, which eventually result in fibrosis, atrophy, progressive scarring and permanent hair loss. Ulerythema ophryogenes begins at birth or soon thereafter; it involves the lateral eyebrows, spreads medially and eventually affects the entire eyebrows, cheeks, and less frequently, forehead and asjecebt scalp. Involvement
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17

Klar, Joakim, Jens Schuster, Tahir Naeem Khan, et al. "Whole exome sequencing identifiesLRP1as a pathogenic gene in autosomal recessive keratosis pilaris atrophicans." Journal of Medical Genetics 52, no. 9 (2015): 599–606. http://dx.doi.org/10.1136/jmedgenet-2014-102931.

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18

Oranje, A. P. "Keratosis pilaris atrophicans. One heterogeneous disease or a symptom in different clinical entities?" Archives of Dermatology 130, no. 4 (1994): 500–502. http://dx.doi.org/10.1001/archderm.130.4.500.

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19

Baden, Howard P. "Clinical Findings, Cutaneous Pathology, and Response to Therapy in 21 Patients With Keratosis Pilaris Atrophicans." Archives of Dermatology 130, no. 4 (1994): 469. http://dx.doi.org/10.1001/archderm.1994.01690040073011.

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20

Baden, H. P. "Clinical findings, cutaneous pathology, and response to therapy in 21 patients with keratosis pilaris atrophicans." Archives of Dermatology 130, no. 4 (1994): 469–75. http://dx.doi.org/10.1001/archderm.130.4.469.

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21

Li, Kayi, Mary Ann Thomas, and Richard M. Haber. "Ulerythema Ophryogenes, A Rarely Reported Cutaneous Manifestation of Noonan Syndrome: Case Report and Review of the Literature." Journal of Cutaneous Medicine and Surgery 17, no. 3 (2013): 212–18. http://dx.doi.org/10.2310/7750.2011.11017.

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Background: Ulerythema ophryogenes (also known as keratosis pilaris atrophicans faciei) is a rarely reported cutaneous manifestation of Noonan syndrome. Objective: Recognizing ulerythema ophryogenes as a cutaneous association in Noonan syndrome may aid in the diagnosis of this relatively common genetic condition. Methods: We present a case of a patient with Noonan syndrome and ulerythema ophryogenes associated with a SOS1 mutation and review the literature on this association. Results: To the best of our knowledge, this is the second case of Noonan syndrome proven to be due to an SOS1 mutation
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22

Gönülal, Melis, Sinem Karaca, and Didem Balcı. "Keratosis Pilaris Atrophicans Faciei: A Case Treated with 585 nm Diode Laser, a Novel Fractional Solid-State." Clinical, Cosmetic and Investigational Dermatology Volume 16 (December 2023): 3497–501. http://dx.doi.org/10.2147/ccid.s441779.

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23

Mao, Qing, Robert Chin, Weiwei Xie, et al. "Advanced Whole-Genome Sequencing and Analysis of Fetal Genomes from Amniotic Fluid." Clinical Chemistry 64, no. 4 (2018): 715–25. http://dx.doi.org/10.1373/clinchem.2017.281220.

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Abstract BACKGROUND Amniocentesis is a common procedure, the primary purpose of which is to collect cells from the fetus to allow testing for abnormal chromosomes, altered chromosomal copy number, or a small number of genes that have small single- to multibase defects. Here we demonstrate the feasibility of generating an accurate whole-genome sequence of a fetus from either the cellular or cell-free DNA (cfDNA) of an amniotic sample. METHODS cfDNA and DNA isolated from the cell pellet of 31 amniocenteses were sequenced to approximately 50× genome coverage by use of the Complete Genomics nanoar
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24

Khetarpal, Shilpi, Apra Sood, and Steven D. Billings. "Nilontinib induced keratosis pilaris atrophicans." Dermatology Online Journal 22, no. 8 (2016). http://dx.doi.org/10.5070/d3228032159.

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25

Fekete, Gyula, László Fekete, Nicoleta Neagu, Vladimir Bacârea, Miruna Drăgănescu, and Ilarie Brihan. "Keratosis pilaris atrophicans faciei: An observational, descriptive, retrospective clinical study." Experimental and Therapeutic Medicine 22, no. 5 (2021). http://dx.doi.org/10.3892/etm.2021.10766.

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26

Elmahi, H., S. Elloudi, S. Gallouj, FZ Mernissi, and M. Rimani. "Keratosis Follicularis Spinulosa Decalvans: A New Observation." February 10, 2017. https://doi.org/10.19070/2332-2977-1700027.

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Keratosis follicularis spinulosa decalvans (KFSD) is a rare condition characterized by diffuse keratosis pilaris with a scarring alopecia of the scalp and associated photophobia, facial erythema, and palmoplantar keratoderma. Although initially described as a sex-linked disorder, several different inheritance patterns have been observed. We describe a patient whose mother and sister were also affected with this condition, consistent with an autosomal dominant genetic transmission. Multiple topical and systemic treatments have been unsuccessful in this patient, attesting to the treatment refrac
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27

S, Soundarya, Brindha J, and Jayakar Thomas. "ATROPHODERMA VERMICULATUM: A RARE CASE WITH ISOLATED PRESENTATION." GLOBAL JOURNAL FOR RESEARCH ANALYSIS, February 15, 2023, 8–9. http://dx.doi.org/10.36106/gjra/1303486.

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Atrophoderma vermiculata is a rare and benign follicular disorder of the skin occurs due to abnormal keratinisation in follicular pilosebaceous unit. It presents as multiple, symmetric, depressed pitted scars with reticular/ honeycomb atrophy of skin. It usually presents in face but in our case lesions are seen over chest, back, shoulder and gluteal region. The onset is mostly sporadic or sometimes inherited Autosomal Dominant. It is a clinical variant of Keratosis Pilaris Atrophicans. This condition is difcult to treat cosmetically. Hereby we report a rare case of Atrophoderma Vermiculatum w
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28

Desai, Deesha D., Ambika Nohria, Jerry Shapiro, and Kristen I. Lo Sicco. "Navigating Diagnostic Uncertainty: Frontal Fibrosing Alopecia Versus Keratosis Pilaris Atrophicans Faciei With Genetic Testing Insights." Cureus, April 23, 2024. http://dx.doi.org/10.7759/cureus.58830.

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