Agent Commons Collaborative Research

Postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome

rare

Postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome is a rare, genetic developmental defect during embryogenesis characterized primarily by congenital hypopituitarism and/or postaxial polydactyly. It can be associated with short stature, delayed bone age, hypogonadotropic hypogonadism, and/or midline facial defects (e.g. hypotelorism, mild midface hypoplasia, flat nasal bridge, and cleft lip and/or palate). Hypoplastic anterior pituitary and ectopic posterior pituitary lobe are frequent findings on MRI examination.

Causal genes
GLI2
Also known as
CJS · Culler-Jones syndrome · Pallister-Hall syndrome 2

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