encyclopedia of medical concepts
ψ 
ψ 
ψ 
ψ 
ψ 
ψ 
ψ 

Weill-Marchesani Syndrome

More information in Books or onNLM PubMed
Definition: Rare congenital disorder of connective tissue characterized by brachydactyly, joint stiffness, childhood onset of ocular abnormalities (e.g., microspherophakia, ECTOPIA LENTIS; GLAUCOMA), and proportionate short stature. Cardiovascular anomalies are occasionally seen.     
See Also Marfan Syndrome
Other names Weill Marchesani Syndrome, Autosomal Recessive; Weill Marchesani Syndrome, Autosomal Dominant; Syndromes, Spherophakia Brachymorphia; Syndromes, Marchesani-Weill; Syndrome, Weill-Marchesani; Syndrome, Spherophakia Brachymorphia; Syndrome, Marchesani-Weill; Spherophakia Brachymorphia Syndromes; Mesodermal Dysmorphodystrophies, Congenital; Marchesani-Weill Syndromes; Marchesani Weill Syndrome; Dysmorphodystrophy, Congenital Mesodermal; Dysmorphodystrophies, Congenital Mesodermal; Congenital Mesodermal Dysmorphodystrophy; Congenital Mesodermal Dysmorphodystrophies; Brachymorphia Syndrome, Spherophakia; Weill-Marchesani Syndrome, Autosomal Dominant; Marchesani-Weill Syndrome; Weill-Marchesani Syndrome, Autosomal Recessive; Weill Marchesani Syndrome

To share this definition, click "text" (Facebook, Twitter) or "link" (blog, mail) then paste text link
Ads by Google

Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

Warning: the drugs or drug combinations referred to here may be similar or related, but are not be the same ones and may not have the same pharmacological action as other substances described on the same page or in the same row. Please refer to product monograph or to your doctor
This website is accredited by Health On the Net Foundation. Click to verify.
We comply with the HONcode standard for trustworthy health information: verify here.
About Reference.MD Privacy