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Focal dermal hypoplasia (Goltz syndrome).
Indian J Dermatol Venereol Leprol ; 2005 Jul-Aug; 71(4): 279-81
Article in English | IMSEAR | ID: sea-53066
ABSTRACT
A 7-year-old girl born of non-consanguineous marriage was evaluated for facial dysmorphism. She had multiple skeletal anomalies like hypoplasia of the right mandible, narrow nasal bridge with broad tip and unilateral notching of the right ala nasi, concomitant squint and low set ears. She also had generalized hypopigmented, atrophic linear macules, multiple papillomas, fat herniations, umbilical hernia, hypoplastic nails, cicatricial alopecia, mild mental retardation, 'lobster-claw' hand and osteopathia striata of long bones, pointing to a diagnosis of Goltz syndrome. The unusual features noted were absence of the left first rib and aortic regurgitation.
Subject(s)
Full text: Available Index: IMSEAR (South-East Asia) Main subject: Pedigree / Abnormalities, Multiple / Severity of Illness Index / Female / Humans / Focal Dermal Hypoplasia / Child / Follow-Up Studies / Risk Assessment / Genetic Predisposition to Disease Type of study: Etiology study / Observational study / Prognostic study / Risk factors Country/Region as subject: Asia Language: English Journal: Indian J Dermatol Venereol Leprol Year: 2005 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Pedigree / Abnormalities, Multiple / Severity of Illness Index / Female / Humans / Focal Dermal Hypoplasia / Child / Follow-Up Studies / Risk Assessment / Genetic Predisposition to Disease Type of study: Etiology study / Observational study / Prognostic study / Risk factors Country/Region as subject: Asia Language: English Journal: Indian J Dermatol Venereol Leprol Year: 2005 Type: Article