Craniomicromelic syndrome: first report in a male
Prakash S Gambhir1, Sunita Gambhir
1Birthright Genetic Clinic, Pune, Maharashtra, India. drprakashgambhir@yahoo.com
American Journal of Medical Genetics. Part A
|February 22, 2011
Abstract:
We report on craniomicromelic syndrome in a male fetus. This case had the previously reported features of prenatal onset growth retardation, underossified cranial bones, wide sutures and fontanels, small face as compared to head, small palpebral fissures, pinched nose, microstomia, micrognathia, and narrow thorax. The consistent combination of these features with short appearing limbs as observed in this case establishes this syndrome as a distinct entity.
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