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Partial trisomy 10(q22-q26) is a extremely rare chromosomal anomaly.
The authors experienced a case of this syndrome in a female newborn infant. She showed
prominent occiput, flat face, blepharophimosis, hypertelorism, lowset ears, micrognathia,
high-arched palate, simian crease on Lt. palm & overlapping of the 5th finger over the 4th finger,
relatively great big toe, and single umbilical artery.Chromosomal study showed the abnormal
chromosome... |
