Microcephaly-brachydactyly-kyphoscoliosis syndrome

Orpha code: 3433OMIM code:

Definicja

Microcephaly-brachydactyly-kyphoscoliosis syndrome is characterized by profound intellectual deficit in association with microcephaly, short stature, brachydactyly type D, a flattened occiput, downslanting palpebral fissures, low-set large ears, a broad prominent nose and kyphoscoliosis. It has been described in three sisters. The disorder is likely to be transmitted as an autosomal recessive trait.

Disease data
Klasyfikacja

Malformation syndrome

Synonimy
Viljoen-Kallis-Voges syndrome
Zespół Viljoena, Kallisa i Vogesa
Kod ORPHA
3433
Kod OMIM
-
Kod ICD10
Q87.8
Kod ICD11
-

No additional description.

Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl