Conradi-Hünermann syndrome


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Conradi-Hünermann syndrome

 [kon-rah´de hu´ner-mahn]
the autosomal dominant form of chondrodysplasia punctata.

Conradi-Hünermann syndrome

(kon-rah'dē hin'ĕr-mahn),
one of the syndromes of chondrodysplasia punctata (q.v.), autosomal dominant, with variable skin keratinization disorders and facial, cardiac, optic, and central nervous system abnormalities; epiphyseal stippling is also present.

Conradi-Hünermann syndrome

[kon·rä′dē· hu′nər·män]
Etymology: Erich Conradi, German physician, 20th century; Carl Hünermann, German physician, 20th century
an autosomal-dominant form of chondrodysplasia punctata, characterized by asymmetric shortening of the limbs and scoliosis, with normal intelligence and life expectancy. The syndrome is also associated with maternal use of warfarin sodium during pregnancy.

Con·ra·di-Hü·ner·mann syn·drome

(kon-rah'dē hyū'nĕr-mahn sin'drōm)
One of the syndromes of chondrodysplasia punctata, autosomal dominant, with variable skin keratinization disorders and facial, cardiac, optic, and central nervous system abnormalities; epiphyseal stippling is also present.