Chondrodysplasia punctata, Toriello type

Orpha code: 79347OMIM code: 215105

Definicja

Chondrodysplasia punctata, Toriello type is a rare, non-rhizomelic, primary bone dysplasia syndrome characterized by calcific stippling of epiphyses in association with minor facial abnormalities, short stature and ocular colobomata. In addition, patients present chondrodysplasia punctata, brachycephaly, flat facial profile with small nose, flat lower eyelids and low-set ears, developmental delay, brachytelephalangy and deep palmar creases. Complex congenital cardiac disease and central nervous system anomalies (including partial absence of corpus callosum, small vermis, enlargement of the cisterna magna and/or of the anterior horns of the lateral ventricles) have been reported.

Disease data
Klasyfikacja

Malformation syndrome

Synonimy
Toriello-Higgins-Miller syndrome
Zespół Toriello, Higginsa i Millera
Kod ORPHA
79347
Kod OMIM
215105
Kod ICD10
Q77.3
Kod ICD11
-

No additional description.

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