B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome

Orpha code: 567502OMIM code:

Definition

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
Classification

Disease

Synonyms
BILU syndrome
Hoffman syndrome
BILU syndrome
Hoffman syndrome
ORPHA code
567502
OMIM code
-
ICD10 code
-
ICD11 code
-

No additional description.

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