Microcephaly-brachydactyly-kyphoscoliosis syndrome

Orpha code: 3433OMIM code:

Definition

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
Classification

Malformation syndrome

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

No additional description.

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