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Marfans Syndrome Wheeless

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Location: http://www.wheelessonline.com/ortho/marfans_syndrome

Description: Discussion: - older names include dolichostenomelia (Greek for long, narrow limbs) and dystrophia mesodermalis congenital, typus Marfanis; - inherited as an autosomal dominant trait with variable expressivity. - characterized by long, thin limbs and by laxity of ligaments;

Type: Reference Material
Author/Contact: Wheeless
Institution: Duke
Primary Subject/Category:

Language: English

Submitted by: admin
Hits: 77
Added: Sun Nov 19 2006