Noonan syndrome with multiple lentigines, abbreviated NSML, is a rare autosomal dominant, multisystem disease caused by a mutation in the PTPN11 gene, which encodes a protein tyrosine phosphatase. It belongs to the group of Ras/MAPK pathway syndromes, the RASopathies. The disease is a complex of features, mostly involving the skin, skeletal and cardiovascular systems, and these may or may not be present in every patient. How the mutation produces each symptom is not well understood and research is continuing. Noonan syndrome is caused by a different missense mutation in the same gene and is fairly common, whereas no epidemiological data exist for NSML.
Facts
Classification
ICD-10 ChapterXVII: Congenital Malformations, Deformations and Chromosomal Abnormalities 2 Communicable or Non-communicable Transmission Route Causative Agent
Causative Agent (category) Prevalence Band Sources
1. Noonan syndrome with multiple lentigines (Wikipedia)
Wikipedia article lead section
caused by a mutation in the protein tyrosine phosphatase, non-receptor type 11 gene (PTPN11)
Wikipedia article lead section [body-system]
mostly involving the skin, skeletal and cardiovascular systems
Wikipedia lead section, inheritance statement
is a rare autosomal dominant, multisystem disease
View the Source2. Orphadata (Orphanet): Orphadata cross-references, ORPHAcode 500
Orphadata (Orphanet)Orphanet cross-reference to ICD-10, chapter derived from the codeQuote, Orphanet cross-reference to ICD-10, chapter derived from the code
"Reference": "Q87.1", "Source": "ICD-10"
View the Source 3. MedlinePlus Genetics (U.S. National Library of Medicine): Noonan syndrome with multiple lentigines - MedlinePlus Genetics
MedlinePlus Genetics (U.S. National Library of Medicine)Description and InheritanceQuote, Description and Inheritance
Noonan syndrome with multiple lentigines is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to
View the Source 4. Orphadata (Orphanet): Orphadata epidemiology, ORPHAcode 500
Orphadata (Orphanet)Orphanet epidemiology, ORPHAcode 500Quote, Orphanet epidemiology, ORPHAcode 500
"PrevalenceClass": "\u003c1 / 1 000 000", "PrevalenceGeographic": "Worldwide", "PrevalenceQualification": "Class only", "PrevalenceType": "Point prevalence"
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