Say-Barber-Miller syndrome

Orpha code: 3132OMIM code: 251240

Definicja

A rare multiple congenital anomalies/dysmorphic syndrome characterized by microcephaly, developmental delay and intellectual disability, postnatal growth retardation, dysmorphic craniofacial features (including sloping forehead, beaked nose, large and protruding ears, micrognathia, high-arched palate, and craniosynostosis), immunologic abnormalities with transient hypogammaglobulinemia in infancy and defective chemotaxis leading to recurrent infections, as well as autoimmune/autoinflammatory phenomena. Skeletal anomalies and hypogonadism have also been reported.

Disease data
Klasyfikacja

Malformation syndrome

Synonimy
Microcephaly-hypogammaglobulinemia-abnormal immunity syndrome
Małogłowie - hipogammaglobulinemia - nieprawidłowa odporność
Kod ORPHA
3132
Kod OMIM
251240
Kod ICD10
Q87.8
Kod ICD11
4A01.0Y

No additional description.

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