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Cardiocutaneous Syndrome: The Tale between Heart and Skin [PDF]

open access: yesGlobal Journal of Rare Diseases, 2017
Cardiocutaneous syndromes are rare, genetically determined disorders in which arrhythmogenic cardiomyopathy is accompanied by characteristic cutaneous phenotypes of woolly hair and palmoplantar keratoderma.
AKMM Islam, A Khan, Z Hossain
exaly   +6 more sources

Cardiocutaneous Syndrome

open access: yes, 2009
Nils Peters   +199 more
exaly   +3 more sources
Some of the next articles are maybe not open access.

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Cardiocutaneous Syndrome Continued

New England Journal of Medicine, 1968
R F, Kraunz, J R, Blackmon
exaly   +3 more sources

Cardiocutaneous Syndrome: Naxos Disease

International Journal of Preclinical and Clinical Research, 2022
Naxos disease is a recessively inherited condition, caused by mutation in genes encoding desmosomal proteins Plakoglobin. It is characterized by peculiar woolly hair, palmoplantar keratoderma with arrhythmogenic Right Ventricular dysplasia /cardiomyopathy.
. Laxmi   +3 more
openaire   +1 more source

Cardiocutaneous syndromes and associations

Journal of the American Academy of Dermatology, 2002
Multiple cardiocutaneous syndromes and associations are described and reviewed with the emphasis on syndromes that are likely first to be recognized by dermatologists, thereby creating awareness of potential significant cardiovascular disease. Multiple lentigines syndrome, the Carney complex, and Marfan syndrome are examples of syndromes with ...
Nagla F, Abdelmalek   +2 more
openaire   +2 more sources

Novel PPP1R13L variant expands the phenotype of a rare cardiocutaneous syndrome

Clinical Genetics, 2022
PPP1R13L-associated cardiocutaneous syndrome is an autosomal recessive condition that presents with life-threatening dilated cardiomyopathy in early childhood, with or without features of inflammation on cardiac histology. There is also a variably expressed ectodermal phenotype.
Asher, Henry   +3 more
openaire   +2 more sources

Atrial myxoma: a cardiocutaneous syndrome

Hospital Medicine, 2004
A52-year-old man presented with recurrent transient ischaemic attacks (TIA), predominantly causing visual disturbance. In the past he had suffered from migraine and had a horseshoe kidney on the right. Additionally, he had previously undergone surgery for several skin lesions (Figures 1a and b) that were myxoid or called 'neurofibromas', although he ...
Simon, Conroy   +4 more
openaire   +2 more sources

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