B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome

Orpha code: 567502OMIM code:

Definicja

A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by almost complete lack of B-cells and severe hypogammaglobulinemia, anomalies of the hands and feet, urogenital malformations, and characteristic facial dysmorphism (including microcephaly, highly arched eyebrows, hypoplastic alae nasi, and micrognathia). Most patients are developmentally normal, although moderate mental retardation has also been described.

Disease data
Klasyfikacja

Disease

Synonimy
BILU syndrome
Hoffman syndrome
BILU syndrome
Hoffman syndrome
Kod ORPHA
567502
Kod OMIM
-
Kod ICD10
-
Kod ICD11
-

No additional description.

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