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Journal articles on the topic 'Keratitis-ichthyosis-deafness'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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1

Madjako, Soumahoro Nina, Fofana Youssouf, Koné Djeneba, et al. "Keratitis - Ichthyosis - Deafness Syndrome (KID): A Case at the Bamako Dermatology Hospital." SAS Journal of Medicine 9, no. 06 (2023): 587–89. http://dx.doi.org/10.36347/sasjm.2023.v09i06.003.

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Summary: The syndrome of keratitis - ichthyosis - deafness (KID) is a rare genetic disorder associating: keratitis, ichthyosis and deafness. We report a case at the dermatology hospital in Bamako (Mali). A 6-month-old boy consulted at the Bamako Dermatology Hospital for a generalized rash evolving since birth associated with psychomotor retardation. Dermatological examination showed warty-looking hyperkeratotic lesions on the trunk, keratoderma palmo -plantar of velvety aspect. Nails were thickened with brown color and onychodysplasia. The axillary folds were the seat of a cupboard covered wit

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2

Nurse, D. S. "Keratitis, ichthyosis, deafness (KID) syndrome." Clinical and Experimental Dermatology 19, no. 3 (1994): 280. http://dx.doi.org/10.1111/j.1365-2230.1994.tb01189.x.

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3

Tsuzuku, Toshihiro, Kimitaka Kaga, Akihiko Shibata, Shuichi Kanematsu, and Schyu Ohde. "Temporal Bone Findings in Keratitis, Ichthyosis, and Deafness Syndrome." Annals of Otology, Rhinology & Laryngology 101, no. 5 (1992): 413–16. http://dx.doi.org/10.1177/000348949210100507.

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In 1981, the term KID syndrome was suggested for patients with congenital ichthyosis associated with deafness and keratitis. We had a chance to examine the temporal bone of an infant with this syndrome. This patient showed no auditory brain stem response in either ear. Temporal bone studies revealed cochleosaccular abnormality. These findings are offered as a possible explanation for the patient's deafness. The pathologic inner ear findings of congenital deafness syndromes associated with ichthyosis have been heretofore reported in Refsum's syndrome and in a case with universal alopecia. In th

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4

Ahmadi, S., and K. McKenna. "Keratitis-ichthyosis-deafness syndrome and carotenaemia." Clinical and Experimental Dermatology 28, no. 4 (2003): 394–96. http://dx.doi.org/10.1046/j.1365-2230.2003.01316.x.

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5

Singh, Kamlender. "KERATITIS, ICHTHYOSIS AND DEAFNESS (KID SYNDROME)." Australasian Journal of Dermatology 28, no. 1 (1987): 38–41. http://dx.doi.org/10.1111/j.1440-0960.1987.tb00329.x.

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6

Reynolds, N. J., and C. T. C. Kennedy. "(4) Keratitis ichthyosis deafness (KID) syndrome." British Journal of Dermatology 123, s37 (1990): 77–80. http://dx.doi.org/10.1111/j.1365-2133.1990.tb04490.x.

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7

McGrae, John D. "Keratitis, Ichthyosis, and Deafness (KID) Syndrome." International Journal of Dermatology 29, no. 2 (1990): 89–93. http://dx.doi.org/10.1111/j.1365-4362.1990.tb04075.x.

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8

Levine, Paul A., Michael R. Morris, Ari Namon, Gary Y. Shaw, William R. Panje, and Ernest E. Mhoon. "The Keratitis, Ichthyosis, and Deafness Syndrome." Otolaryngology–Head and Neck Surgery 104, no. 4 (1991): 526–28. http://dx.doi.org/10.1177/019459989110400417.

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9

Miteva, Ljubka. "Keratitis, Ichthyosis, and Deafness (KID) Syndrome." Pediatric Dermatology 19, no. 6 (2002): 513–16. http://dx.doi.org/10.1046/j.1525-1470.2002.00222.x.

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10

Mazereeuw-Hautier, J. "Syndrome de keratitis-ichthyosis-deafness (KID)." Annales de Dermatologie et de Vénéréologie 135, no. 1 (2008): 80–82. http://dx.doi.org/10.1016/j.annder.2007.11.013.

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11

Mazereeuw-Hautier, J. "Syndrome de keratitis-ichthyosis-deafness (KID)." Annales de Dermatologie et de Vénéréologie 135, no. 1 (2008): 79. http://dx.doi.org/10.1016/j.annder.2007.12.004.

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12

Mazereeuw-Hautier, J. "Syndrome de keratitis-ichthyosis-deafness (KID)." Annales de Dermatologie et de Vénéréologie 135, no. 1 (2008): 83. http://dx.doi.org/10.1016/j.annder.2007.12.005.

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13

Grob, Jean Jacques. "Keratitis, Ichthyosis, and Deafness (KID) Syndrome." Archives of Dermatology 123, no. 6 (1987): 777. http://dx.doi.org/10.1001/archderm.1987.01660300099020.

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14

Fozza, Claudio, Fausto Poddie, Salvatore Contini, et al. "Keratitis-Ichthyosis-Deafness Syndrome, Atypical Connexin GJB2 Gene Mutation, and Peripheral T-Cell Lymphoma: More Than a Random Association?" Case Reports in Hematology 2011 (2011): 1–3. http://dx.doi.org/10.1155/2011/848461.

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Keratitis-ichthyosis-deafness (KID) syndrome is a rare congenital disorder characterized by skin lesions, neurosensorial hypoacusia, and keratitis, usually due to the mutation involving the connexin 26 gene. We report on a KID patient who showed the atypical mutation and developed a T-cell lymphoma so far never described in this group of patients.

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15

KIM, Beom Joon, Yeon Jin KIM, Kwang Ho YOO, et al. "Keratitis-ichthyosis-deafness syndrome with unusual hypopigmentation." Journal of Dermatology 35, no. 12 (2008): 798–800. http://dx.doi.org/10.1111/j.1346-8138.2008.00574.x.

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16

Okmen, Fırat, Ismet Hortu, Ulduz Jafarova, Metehan Imamoglu, Huseyin Ekici, and Ahmet Mete Ergenoglu. "Antenatal Findings of Keratitis-Ichthyosis-Deafness Syndrome." Journal of Obstetrics and Gynaecology Canada 42, no. 4 (2020): 504–6. http://dx.doi.org/10.1016/j.jogc.2019.06.005.

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17

de Berker, David, William A. Branford, Sava Soucek, and Leslie Michaels. "Fatal Keratitis Ichthyosis and Deafness Syndrome (KIDS)." American Journal of Dermatopathology 15, no. 1 (1993): 64–69. http://dx.doi.org/10.1097/00000372-199302000-00012.

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18

Binder, Barbara, Hans Christian Hennies, Raimund Kraschl, and Josef Smolle. "Connexin-26-Mutation bei "Keratitis-Ichthyosis-Deafness"-Syndrom (KID-Syndrom). Connexin 26 mutation and keratitis-ichthyosis-deafness (KID) Syndrome." Journal der Deutschen Dermatologischen Gesellschaft 3, no. 2 (2005): 105–8. http://dx.doi.org/10.1111/j.1610-0378.2005.04748.x.

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19

Lonhare, Rahul Kumar, Imran Ansari, Preeti Sahu, and Debadatta Mahallik. "An audiological profile of keratitis-ichthyosis-deafness syndrome." International Journal of Research in Medical Sciences 10, no. 9 (2022): 2047. http://dx.doi.org/10.18203/2320-6012.ijrms20222288.

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Keratitis-ichthyosis-deafness (KID) syndrome is a rare genetic multi-system disorder. It is characterized by defects of the surface of the corneas (keratitis), red, rough thickened plaques of skin (erythrokeratoderma) with sensorineural hearing impairment. The skin of the palms of the hand, soles of the feet and the nails may be affected. Most cases are sporadic caused by mutations in the (GJB2 gene). Most cases are sporadic but familial cases with autosomal dominant inheritance have been reported a rare congenital ectodermal disorder characterized by vascularising keratitis hyperkeratotic ski

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20

Stepanović, Milica, Mirjana Paravina, Goran Janković, and Danica Janjić Spasić. "Keratitis, Ichthyosis and Deafness (KID) Syndrome – a Case Report." Serbian Journal of Dermatology and Venerology 5, no. 1 (2013): 22–30. http://dx.doi.org/10.2478/sjdv-2013-0003.

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Abstract Keratitis, ichthyosis and deafness (KID) syndrome is a rare congenital ectodermal dysplasia characterized by ichthyosiform hyperkeratosis of the skin, neurosensory hearing loss and vascularizing keratitis. It is inherited as an autosomal dominant trait, now known to be due to mutations in the connexin gene. This paper presents a case of a 20-year-old male patient with erythrokeratodermia and mild scaling since birth. He presented mild hearing impairment at the age of two and often suffered from eye inflammations. On admission, his clinical picture was typical of KID syndrome with eryt

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21

Shanker, Vinay, Mudita Gupta, and Aditi Prashar. "Keratitis-Ichthyosis-Deafness syndrome: A rare congenital disorder." Indian Dermatology Online Journal 3, no. 1 (2012): 48. http://dx.doi.org/10.4103/2229-5178.93505.

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22

NAGATA, Yoshiko, Yuko HIGASHI, Hisashi KAWABATA, Yuki FUKUDOME, and Tamotsu KANZAKI. "A Case of KID(Keratitis, Ichthyosis, Deafness) Syndrome." Nishi Nihon Hifuka 62, no. 1 (2000): 23–27. http://dx.doi.org/10.2336/nishinihonhifu.62.23.

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23

Szymko-Bennett, Yvonne M., Laura J. Russell, Sherri J. Bale, and Andrew J. Griffith. "Auditory Manifestations of Keratitis-Ichthyosis-Deafness (KID) Syndrome." Laryngoscope 112, no. 2 (2002): 272–80. http://dx.doi.org/10.1097/00005537-200202000-00014.

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24

Messmer, E. M., K. R. Kenyon, O. Rittinger, A. R. Janecke, and A. Kampik. "Ocular manifestations of keratitis– ichthyosis–deafness (KID) syndrome." Ophthalmology 112, no. 2 (2005): e1-e6. http://dx.doi.org/10.1016/j.ophtha.2004.07.034.

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25

Watanabe, Daisuke, Mcasahiro Zako, Yasuhiko Tamada, and Yoshinari Matsumoto. "A case of keratitis?ichthyosis?deafness (KID) syndrome." International Journal of Dermatology 46, no. 4 (2007): 400–402. http://dx.doi.org/10.1111/j.1365-4632.2007.03170.x.

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26

Jurecka, W. "Keratitis, ichthyosis, and deafness syndrome with glycogen storage." Archives of Dermatology 121, no. 6 (1985): 799–801. http://dx.doi.org/10.1001/archderm.121.6.799.

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27

Jurecka, Wolfgang. "Keratitis, Ichthyosis, and Deafness Syndrome With Glycogen Storage." Archives of Dermatology 121, no. 6 (1985): 799. http://dx.doi.org/10.1001/archderm.1985.01660060113034.

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28

Nazzaro, Vincenzo, Claudine Blanchet-Bardon, Gérard Lorette, and Jean Civatte. "Familial occurrence of KID (keratitis, ichthyosis, deafness) syndrome." Journal of the American Academy of Dermatology 23, no. 2 (1990): 385–88. http://dx.doi.org/10.1016/0190-9622(90)70229-b.

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29

Nemoto-Hasebe, Ikue, Masashi Akiyama, Nanako Yamada, Yoshitsugu Inoue, Chizu Touge, and Hiroshi Shimizu. "Keratitis-Ichthyosis-Deafness Syndrome Lacking Subjective Hearing Impairment." Acta Dermato-Venereologica 88, no. 4 (2008): 406–8. http://dx.doi.org/10.2340/00015555-0457.

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30

Kharodawala, Mariya, Shekhar N. Pradhan, Anil Gosavi, and Sunil Tolat. "The Enigma of a Keratitis-Ichthyosis-Deafness with Silence, Scaling, and Related Syndrome." Indian Journal of Paediatric Dermatology 24, no. 4 (2023): 291–94. http://dx.doi.org/10.4103/ijpd.ijpd_13_23.

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Abstract Ichthyosis is a group of genetic disorders characterized by generalized dry skin and scaling, and it can be frequently associated with erythroderma. Here, we report a case of ichthyosis associated with a rare syndrome. A 6-year-old congenitally deaf female presented with severe scaling and generalized erythema for 6 months which began with a scaly plaque over the face at the age of 18 months and gradually covered the whole body. Three similar episodes happened after that with a gap of 6 months. There were multiple scaly erythematous plaques present over the trunk and limbs and thick h

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31

McGrae, John D. "Keratitis, Ichthyosis, and Deafness (KID) Syndrome with Adult Onset of Keratitis Component." International Journal of Dermatology 29, no. 2 (1990): 145–46. http://dx.doi.org/10.1111/j.1365-4362.1990.tb04090.x.

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32

Vyas, HarshitaRavindra, ShikhaR Shah, UmeshK Karia, and BelaJ Shah. "Keratitis–Ichthyosis–Deafness: A rare kid in clinical practice." Indian Journal of Paediatric Dermatology 23, no. 3 (2022): 251. http://dx.doi.org/10.4103/ijpd.ijpd_31_22.

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33

Perez-Rueda, Antonio, Rocío Melero-Giménez, Almudena Valero-Marcos, Javier Fernández-Castro, Jesús Martín-Molina, and Gracia Castro-Luna. "Keratitis–ichthyosis–deafness (KID) syndrome: Ocular manifestations and management." Indian Journal of Ophthalmology - Case Reports 1, no. 4 (2021): 619. http://dx.doi.org/10.4103/ijo.ijo_3703_20.

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34

MOHRENSCHLAGER, MATTHIAS, JOHANNES RING, and DIETRICH ABECK. "ADDITIONAL ASPECTS OF KERATITIS, ICHTHYOSIS, AND DEAFNESS (KID) SYNDROME." Pediatric Dermatology 21, no. 4 (2004): 518–19. http://dx.doi.org/10.1111/j.0736-8046.2004.21431.x.

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35

Hsu, Huan-Chang, Guan-Shayn Lin, and Wei-Min Li. "Keratitis, Ichthyosis, and Deafness (KID) Syndrome With Cerebellar Hypoplasia." International Journal of Dermatology 27, no. 10 (1988): 695–97. http://dx.doi.org/10.1111/j.1365-4362.1988.tb01266.x.

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36

Koné-Paut, Isabelle, Sylvie Hesse, Christian Palix, et al. "Keratitis, Ichthyosis, and Deafness (KID) Syndrome in Half Sibs." Pediatric Dermatology 15, no. 3 (2009): 219–21. http://dx.doi.org/10.1111/j.1525-1470.1998.tb01320.x.

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37

Conrado, Luciana A., Silvio A. Marques, Joel C. Lastoria, Luís Carlos Cucé, Mariangela E. A. Marques, and Neusa L. Dillon. "Keratitis-ichthyosis-deafness (KID) syndrome with squamous cell carcinoma." International Journal of Dermatology 46, no. 4 (2007): 403–6. http://dx.doi.org/10.1111/j.1365-4632.2007.02977.x.

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38

Mayama, H., T. Fujimura, M. Asano, Y. Kambayashi, Y. Numata, and S. Aiba. "Squamous Cell Carcinoma Arising from Keratitis–Ichthyosis–Deafness Syndrome." Acta Dermato Venereologica 93, no. 5 (2013): 583–84. http://dx.doi.org/10.2340/00015555-1535.

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39

Titeux, Matthias, Vanessa Mendonça, Audrey Décha, et al. "Keratitis-Ichthyosis-Deafness Syndrome Caused by GJB2 Maternal Mosaicism." Journal of Investigative Dermatology 129, no. 3 (2009): 776–79. http://dx.doi.org/10.1038/jid.2008.312.

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40

Holobradá, M. "Keratitis, ichthyosis, and deafness (KID) syndrome: a case report." Journal of the European Academy of Dermatology and Venereology 5, no. 1 (1995): S142. http://dx.doi.org/10.1016/0926-9959(95)96342-6.

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41

Derelioglu, Sera Sımsek, Yücel Yılmaz, and Sultan Keles. "Dental Treatments under the General Anesthesia in a Child with Keratitis, Ichthyosis, and Deafness Syndrome." Case Reports in Dentistry 2013 (2013): 1–6. http://dx.doi.org/10.1155/2013/618468.

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KID syndrome is a rare genodermatosis characterized by keratitis, ichthyosis, and sensorineural deafness. Although the dermatological, ophthalmologic, and sensorineural defects are emphasized in the literature, oral and dental evaluations are so superficial. In this case report, dental and oral symptoms of a three year and five months old boy with KID syndrome, suffering severe Early Childhood Caries (s-ECC) and dental treatments done under General Anesthesia (GA) were reported.

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42

KANWAR, A. J., S. GHOSH, S. HANDA, G. P. THAMI, and S. KAUR. "Keratitis, ichthyosis, deafness (KID) syndrome-the first report from India." Clinical and Experimental Dermatology 18, no. 4 (1993): 386–88. http://dx.doi.org/10.1111/j.1365-2230.1993.tb02227.x.

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43

Bartenstein, Diana, Hye Jin Chung, and Sadaf Hussain. "Two Cases of Chronic Candidiasis in Keratitis–Ichthyosis–Deafness Syndrome." American Journal of Dermatopathology 40, no. 10 (2018): e138-e141. http://dx.doi.org/10.1097/dad.0000000000001178.

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44

Ma, Han, Panpan Liang, Jian Chen, Peiying Feng, and Wei Lai. "Keratitis-ichthyosis-deafness syndrome accompanied by disseminated cutaneous fungal infection." Journal of Dermatology 44, no. 11 (2017): 1255–61. http://dx.doi.org/10.1111/1346-8138.13926.

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45

Lee Lenis, Tamara, Wenlin Zhang, Vivian Shibayama, et al. "Mulitmodal Corneal Imaging of Genetically Confirmed Keratitis–Ichthyosis–Deafness Syndrome." Cornea 39, no. 11 (2020): 1446–49. http://dx.doi.org/10.1097/ico.0000000000002415.

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46

Dengler, S., V. Oji, A. Lücke, V. Schindler, D. Nashan, and H. Ständer. "Keratitis-ichthyosis-deafness (KID)-Syndrom – Fallbericht einer seltenen hereditären Ichthyoseform." Aktuelle Dermatologie 42, no. 08/09 (2016): 332–35. http://dx.doi.org/10.1055/s-0042-108020.

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47

Bhattarai, Sabina, Arti S. Pandey, Sherya Bastakoti, Peter Soderkvist, and Mohan Bhusal. "A case of keratitis, ichthyosis, and deafness syndrome with rickets." JAAD Case Reports 6, no. 1 (2020): 9–12. http://dx.doi.org/10.1016/j.jdcr.2019.10.024.

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48

Janecke, Andreas R., Hans Christian Hennies, Barbara Günther, et al. "GJB2mutations in keratitis-ichthyosis-deafness syndrome including its fatal form." American Journal of Medical Genetics Part A 133A, no. 2 (2005): 128–31. http://dx.doi.org/10.1002/ajmg.a.30515.

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49

Nowell, W. A. "Keratitis, ichthyosis, and deafness (KID) syndrome: suggested changes in terminology." Archives of Dermatology 124, no. 1 (1988): 22b—22. http://dx.doi.org/10.1001/archderm.124.1.22b.

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50

Myskowski, Patricia L. "Keratitis, Ichthyosis, and Deafness (KID) Syndrome: Suggested Changes in Terminology." Archives of Dermatology 124, no. 1 (1988): 22. http://dx.doi.org/10.1001/archderm.1988.01670010012006.

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