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Postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome
rarePostaxial 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.
- Identifiers
- MONDO:0014369 OMIM:615849Orphanet:420584
- Causal genes
- GLI2
- Part of
- Autosomal dominant diseaseCongenital limb malformationDysostosisNon-acquired combined pituitary hormone deficiencySyndromic disease
- Also known as
- CJS · Culler-Jones syndrome · Pallister-Hall syndrome 2
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