Acromesomelic dysplasia, Hunter-Thompson type

Orpha code: 968OMIM code: 201250

Definicja

A rare autosomal recessive acromesomelic dysplasia characterized by severe dwarfism (adult height approximately 120 cm) with abnormalities limited to the limbs (affecting the lower limbs more than upper limbs, with middle and distal segments being the most affected), severe shortening, absence or fusion of tubular bones of hands and feet and large joint dislocations. As seen in acromesomelic dysplasia, Grebe type and acromesomelic dysplasia, Maroteaux type, facial features and intelligence are normal.

Disease data
Klasyfikacja

Malformation syndrome

Synonimy
Acromesomelic dwarfism
Karłowatość akromezomeliczna
Kod ORPHA
968
Kod OMIM
201250
Kod ICD10
Q78.8
Kod ICD11
LD24.9

No additional description.

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