Noonan syndrome (male turner syndrome) 8

Noonan Syndrome (Male Turner Syndrome) 131j97b 131j97b 131j97b 131j97b 8

General: Similar to Turner syndrome, but with normal chromosomal analysis; X-linked dominant inheritance; X-linked dominant phenotype.

Ocular: Hypertelorism; exophthalmos; ptosis (unilateral or bilateral); antimongoloid-slanting palpebral fissure; myopia; keratoconus; optic disk coloboma.

Clinical: Valvular pulmonary stenosis; short stature; webbed neck; low hairline in the back; cubitus valgus; deformed chest wall; micrognathia; low-set ears; mild mental retardation.

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