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Wolf-Hirschhorn syndrome was first described in 1961 by two physicians, Dr. Carl Wolfgang and Dr. Eberhard Hirschhorn, who identified the condition in a group of affected individuals. This genetic disorder is characterized by a deletion of a segment of chromosome 4, leading to various physical and developmental challenges. The syndrome is associated with distinctive facial features, growth delays, and intellectual disabilities. Subsequent research has further elucidated the genetic basis and clinical manifestations of the syndrome.

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AnswerBot

6d ago

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