dolichostenomelia
Sign in to saveAlso known as disproportionate tall stature
Dolichostenomelia is a human condition in which the limbs are unusually long. The name is derived . It is a common feature of several kinds of hereditary disorders which affect connective tissue, such as Marfan syndrome and homocystinuria.
In the Vinony graph
Within Vinony's link graph, dolichostenomelia is referenced by 4 other articles, and connects out to medicine, disease and physician.
It is catalogued under the topic Musculoskeletal disorders.
Its subject is documented across 5 Wikipedia language editions.
Clinical Trials
84 registered- ACTIVE_NOT_RECRUITINGMarfan Syndrome and Quality of Life of Pediatric PatientsIRCCS Policlinico S. Donato · NCT05748314
- COMPLETEDTowards Optimal Treatment of Marfan SyndromeAcademisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) · NCT05944614
- COMPLETEDNonlinear Elasticity Mapping of Breast MassesMayo Clinic · NCT04863443
- NANOT_YET_RECRUITINGNutritional Ketosis MarfanWashington University School of Medicine · NCT07495267
- PHASE3COMPLETEDRandomized, Double-blind Study for the Evaluation of the Effect of Losartan Versus Placebo on Aortic Root Dilatation in Patients With Marfan Syndrome Under Treatment With Beta-blockersUniversity Hospital, Ghent · NCT00782327
- UNKNOWNPsychological Support in Adult Patients With Marfan SyndromeIRCCS Policlinico S. Donato · NCT05712577
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Encyclopedic overview
1 sectionsContents
- References
Dolichostenomelia is a human condition in which the limbs are unusually long. The name is derived . It is a common feature of several kinds of hereditary disorders which affect connective tissue, such as Marfan syndrome and homocystinuria.
==References==
Excerpted from Wikipedia’s “dolichostenomelia” article, available under the CC BY-SA 4.0 licence.