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Say-Barber-Miller syndrome

ORPHA:3132· ICD-10 Q87.8

Definition

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.

Prevalence
<1 / 1 000 000
Inheritance
Unknown
Age of onset
Antenatal, Infancy, Neonatal