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Tatton-Brown-Rahman syndrome

ORPHA:404443· ICD-10 Q87.3

Definition

A rare multiple congenital anomalies syndrome characterized by tall stature due to postnatal overgrowth, mild to moderate intellectual disability, joint hypermobility and subtle distinctive facial features, which often become apparent during adolescence (such as round face, low-set, thick horizontal eyebrows, narrow palpebral fissures and prominent upper-central incisors). Overweight, hypotonia, behavioral and psychiatric problems are common. Other clinical features may involve seizures, cryptorchidism and cardiovascular diseases (including congenital heart disease and aortic root dilatation).

Prevalence
<1 / 1 000 000
Inheritance
Autosomal dominant
Age of onset
Neonatal