Persistent falcine sinus and unilateral renal agenesis in a girl with Sotos syndrome.

CLINICAL DYSMORPHOLOGY(2011)

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摘要
Sotos syndrome is an overgrowth syndrome characterized by distinctive facial features, developmental delay, and macrocephaly. Here, we present a 10-year-old girl with prenatal and postnatal overgrowth, prominent forehead, pointed chin, and advanced bone age. She also has a persistent falcine sinus in the posterior falx cerebri, patent ductus arteriosus, unilateral renal agenesis, and scoliosis. A pituitary macroadenoma was also found with external compression of the inferior aspect of the optic chiasm. We identified a de novo missense mutation of the NSD1 (nuclear receptor-binding SET domain protein 1) gene in this patient. Computational three-dimensional structural analysis revealed that the NSD1 mutation induced major alterations. Clin Dysmorphol 20:42-46 (C) 2011 Wolters Kluwer Health | Lippincott Williams & Wilkins.
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falcine sinus,macroadenoma,missense mutation,nuclear receptor binding SET domain protein 1 gene,renal agenesis,Sotos syndrome
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