Abstract |
We report a case of KID syndrome in a young girl born to non-consanguinous parents without any similar family history. The typical features of this dysplasia, erythrokeratodermia with dry rugous teguments, pachydermia folds of the knees, facial erythema, peribuccal grooves, leucokeratosic perleche, hypotrichosis of the eye lashes and eyebrows, early onset deafness and ophtalmological lesions were observed. The characteristic pachydermatoglyphia of the hands was present. A malformation of the posterior cerebral fossa--a dandy walker syndrome--was revealed at computed tomography.
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Authors | O Boudghene-Stambouli, A Merad-Boudia, S Abdelali |
Journal | Annales de dermatologie et de venereologie
(Ann Dermatol Venereol)
Vol. 121
Issue 2
Pg. 99-102
( 1994)
ISSN: 0151-9638 [Print] France |
Vernacular Title | KID-syndrome, pachydermatoglyphie et syndrome du Dandy Walker. |
PMID | 7979040
(Publication Type: Case Reports, Journal Article)
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Topics |
- Abnormalities, Multiple
- Child
- Dandy-Walker Syndrome
(complications, diagnostic imaging)
- Deafness
(complications, congenital)
- Female
- Humans
- Ichthyosiform Erythroderma, Congenital
(complications)
- Keratitis
(complications, congenital)
- Keratoderma, Palmoplantar
(complications, congenital)
- Syndrome
- Tomography, X-Ray Computed
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