Hyperphosphatasia-intellectual disability syndrome

Orpha code: 247262OMIM code: 616809

Definition

A rare, congenital disorder of glycosylation-related bone disorder characterized by hypotonia, severe developmental delay, intellectual disability, seizures, increased serum alkaline phosphatase, short distal phalanges with hypoplastic nails, and dysmorphic facial features. In some cases, cleft palate, megacolon, anorectal malformations, and congenital heart defects have been reported.

Disease data
Classification

Disease

Synonyms
Mabry syndrome
HPMR
Zespół Mabry'ego
ORPHA code
247262
OMIM code
616809
ICD10 code
Q87.8
ICD11 code
-

No additional description.

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