An autosomal dominant disorder with an acronym of its seven features (LENTIGO; ELECTROCARDIOGRAM abnormalities; ocular HYPERTELORISM; PULMONARY STENOSIS; abnormal genitalia; retardation of growth; and DEAFNESS or SENSORINEURAL HEARING LOSS). This syndrome is caused by mutations of PTPN11 gene encoding the non-receptor PROTEIN TYROSINE PHOSPHATASE, type 11, and is an allelic to NOONAN SYNDROME. Features of LEOPARD syndrome overlap with those of NEUROFIBROMATOSIS 1 which is caused by mutations in the NEUROFIBROMATOSIS 1 GENES.
See also reference (FX) in Slovak
neurofibromatóza 1 Noonanovej syndróm
See also reference (FX) in English
Neurofibromatosis 1 Noonan Syndrome
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(4) - ARTICLES
(2) - MeSH descriptor
subject heading
openseadragon
Number of the records: 1
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