Перевод и анализ слов искусственным интеллектом
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- этимология
LEOPARD syndrome - перевод на арабский
![Hand of 37-year-old patient showing [[interdigital webbing]]](https://commons.wikimedia.org/wiki/Special:FilePath/Leopardsyn2e.jpg?width=200 "Hand of 37-year-old patient showing [[interdigital webbing]]")
![Thirty-seven-year-old patient demonstrating [[hyperelasticity]]](https://commons.wikimedia.org/wiki/Special:FilePath/Leopardsyn2f.jpg?width=200 "Thirty-seven-year-old patient demonstrating [[hyperelasticity]]")
![21-month-old, third generation patient, confirmed by genetic tests as [https://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176876&a=176876_AllelicVariant0005 Y279C], exhibiting ocular hyperteliorism, cephalofacial similarity.](https://commons.wikimedia.org/wiki/Special:FilePath/Leopardsyn3.jpg?width=200 "21-month-old, third generation patient, confirmed by genetic tests as [https://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176876&a=176876_AllelicVariant0005 Y279C], exhibiting ocular hyperteliorism, cephalofacial similarity.")
![[[Torso]] of thirty-seven-year-old, second-generation patient, exhibiting [[lentiginosis]].](https://commons.wikimedia.org/wiki/Special:FilePath/Leopardsyn2b.jpg?width=200 "[[Torso]] of thirty-seven-year-old, second-generation patient, exhibiting [[lentiginosis]].")
Определение
Википедия
Noonan syndrome with multiple lentigines (NSML) which is part of a group called Ras/MAPK pathway syndromes, is a rare autosomal dominant, multisystem disease caused by a mutation in the protein tyrosine phosphatase, non-receptor type 11 gene (PTPN11). The disease is a complex of features, mostly involving the skin, skeletal and cardiovascular systems, which may or may not be present in all patients. The nature of how the mutation causes each of the condition's symptoms is not well known; however, research is ongoing. It is a RASopathy.
Noonan syndrome with multiple lentigines is caused by a different missense mutation of the same gene. Noonan syndrome is fairly common (1:1,000 to 1:2,500 live births), and neurofibromatosis 1 (which was once thought to be related to NSML) is also common (1:3500); however, no epidemiological data exists for NSML.
