Dobrow syndrome

Orpha code: 3262OMIM code:

Definition

A rare multiple congenital defects/dysmorphic syndrome characterized by variable degrees of bony syngnathia associated with variable additional abnormalities, including growth retardation, intellectual disability, microcephaly, iris coloboma, nystagmus, deafness, and vertebral segmentation defects, as well as genital, limb and additional facial malformations, among others.

Disease data
Classification

Malformation syndrome

Synonyms
Syngnathia-multiple anomalies syndrome
ORPHA code
3262
OMIM code
-
ICD10 code
Q87.8
ICD11 code
-

No additional description.

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