Keyword Analysis & Research: marfanoid habitus

nih.gov

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8775541/

WEBJan 11, 2022 · Discussion. Marfan syndrome is a disease with a severe clinical course. The most common cause of mortality in MFS is progressive aortic root dilatation, which can lead to dissection or rupture of the aorta. Aortic root dilatation is found in about 75% of children and 85% of adults with MFS [ 8 ].

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wikipedia.org

https://en.wikipedia.org/wiki/Marfanoid

WEBMarfanoid (or Marfanoid habitus) is a constellation of signs resembling those of Marfan syndrome, including long limbs, with an arm span that is at least 1.03 of the height of the individual, and a crowded oral maxilla, sometimes with a high arch in the palate, arachnodactyly, and hyperlaxity.

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mayoclinic.org

https://www.mayoclinic.org/diseases-conditions/marfan-syndrome/symptoms-causes/syc-20350782

WEBMar 22, 2024 · Marfan syndrome is an inherited disorder that affects connective tissue — the fibers that support and anchor your organs and other structures in your body. Marfan syndrome most commonly affects the heart, eyes, blood vessels and skeleton. People with Marfan syndrome are usually tall and thin with unusually long arms, legs, fingers and toes. marfanoid

marfanoid

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mdpi.com

https://www.mdpi.com/1660-4601/19/2/772

WEBJan 11, 2022 · Marfan syndrome; marfanoid habitus; thumb sign; wrist sign; pectus carinatum; pectus excavatum; gothic palate; Ghent criteria; aortic root dilatation. 1. Introduction. Marfan Syndrome (MFS) is an autosomal dominant systemic disorder caused by mutations in the extracellular matrix protein: fibrillin-1 (FBN1).

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nature.com

https://www.nature.com/articles/nrrheum.2013.24

WEBMar 12, 2013 · Although the marfanoid habitus is primarily associated with Marfan syndrome (MFS), MFS is only one potential diagnosis. In particular, joint hypermobility syndrome (JHS), a far more prevalent...

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nih.gov

https://pubmed.ncbi.nlm.nih.gov/35055593/

WEBJan 11, 2022 · Abstract. Marfan Syndrome (MFS) is a systemic disorder caused by mutations in fibrillin-1. The most common cause of mortality in MFS is dissection and rupture of the aorta. Due to a highly variable and age-dependent clinical spectrum, the diagnosis of MFS still remains sophisticated.

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marfan.org

https://marfan.org/conditions/marfan-syndrome/

WEBMarfan syndrome is a genetic condition that affects the body’s connective tissue. Connective tissue holds all the body’s cells, organs and tissue together. It also plays an important role in helping the body grow and develop properly. What is Marfan Syndrome? Key Features. Causes. Getting Diagnosed. Management. Pregnancy. Emergency … marfanoid

marfanoid

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nih.gov

https://www.ncbi.nlm.nih.gov/books/NBK1335/

WEBApr 18, 2001 · FBN1 -related Marfan syndrome (Marfan syndrome), a systemic disorder of connective tissue with a high degree of clinical variability, comprises a broad phenotypic continuum ranging from mild (features of Marfan syndrome in one or a few systems) to severe and rapidly progressive neonatal multiorgan disease.

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mdpi.com

https://www.mdpi.com/1660-4601/19/2/772/review_report

WEBHow to Distinguish Marfan Syndrome from Marfanoid Habitus in a Physical Examination—Comparison of External Features in Patients with Marfan Syndrome and Marfanoid Habitus. Int. J. Environ. Res. Public Health 2022, 19 (2), 772; https://doi.org/10.3390/ijerph19020772.

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nature.com

https://www.nature.com/articles/jhg20071

WEBOct 24, 2006 · Typical MFS can affect the skeletal system (marfanoid habitus including arachnodactyly, dolichostenomelia, pectus deformity and scoliosis), the ocular system (ectopia lentis) and the...

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