Germline mosaicism in keratitis-ichthyosis-deafness syndrome: pre-natal diagnosis in a familial lethal form

Author:

Sbidian E,Feldmann D,Bengoa J,Fraitag S,Abadie V,de Prost Y,Bodemer C,Hadj-Rabia S

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference20 articles.

1. The keratitis, ichthyosis, and deafness (KID) syndrome;Skinner;Arch Dermatol,1981

2. Keratitis, ichthyosis, and deafness (KID syndrome): review of the literature and proposal of a new terminology;Caceres-Rios;Pediatr Dermatol,1996

3. Keratitis, hepatitis, ichthyosis, and deafness: report and review of KID syndrome;Wilson;Am J Med Genet,1991

4. Dry congenital erythroderma ichthyosiforme, deaf-mutism, and hepatomegaly of recessive autosomal transmission. Study of a family.;Desmons;Bull Soc Fr Dermatol Syphiligr,1971

5. Keratitis-ichthyosis-deafness syndrome: disease expression and spectrum of connexion 26 (GJB2) mutations in 14 patients;Mazereeuw-Hautier;Br J Dermatol,2007

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