| VCF s. |
an autosomal dominant syndrome of cardiac defects and characteristic craniofacial abnormalities including cleft palate, jaw abnormalities, and prominent nose; it is often associated with abnormalities of chromosome 22. Learning disabilities occur often; short stature, slender hyperextensible hands and digits, scoliosis, mental retardation, inguinal hernia, auricular abnormalities, and microcephaly occur less frequently. Called also Shprintzen's s.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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