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  2. Noonan syndrome - Wikipedia

    en.wikipedia.org/wiki/Noonan_syndrome

    Noonan syndrome is the second most common syndromic cause of congenital heart disease. 50-70% of individuals with NS are born with some form of congenital heart defect, with pulmonary valvular stenosis being the most common (50–60%). [9]

  3. Jacqueline Noonan - Wikipedia

    en.wikipedia.org/wiki/Jacqueline_Noonan

    Jacqueline Anne Noonan (October 28, 1928 – July 23, 2020) was an American pediatric cardiologist best known for her characterization of a genetic disorder now called Noonan syndrome. [ 1 ] [ 2 ] She was also the original describer of hypoplastic left heart syndrome .

  4. List of genetic disorders - Wikipedia

    en.wikipedia.org/wiki/List_of_genetic_disorders

    The following is a list of genetic disorders and if known, type of mutation and for the chromosome involved. Although the parlance "disease-causing gene" is common, it is the occurrence of an abnormality in the parents that causes the impairment to develop within the child. There are over 6,000 known genetic disorders in humans.

  5. Noonan syndrome with multiple lentigines - Wikipedia

    en.wikipedia.org/wiki/Noonan_syndrome_with...

    Noonan syndrome with multiple lentigines (NSML) which is part of a group called Ras/MAPK pathway syndromes, [2] is a rare autosomal dominant, [3] multisystem disease caused by a mutation in the protein tyrosine phosphatase, non-receptor type 11 gene . The disease is a complex of features, mostly involving the skin, skeletal and cardiovascular ...

  6. Webbed neck - Wikipedia

    en.wikipedia.org/wiki/Webbed_neck

    Medical genetics: A webbed neck, ... It is a feature of Turner syndrome [1] (only found in girls) and Noonan syndrome, [2] ...

  7. Short-stature homeobox gene - Wikipedia

    en.wikipedia.org/wiki/Short-stature_homeobox_gene

    n/a Ensembl ENSG00000185960 n/a UniProt O15266 n/a RefSeq (mRNA) n/a n/a RefSeq (protein) NP_000442 NP_006874 n/a Location (UCSC) n/a n/a PubMed search n/a Wikidata View/Edit Human The short-stature homeobox gene (SHOX), also known as short-stature-homeobox-containing gene, is a gene located on both the X and Y chromosomes, which is associated with short stature in humans if mutated or present ...

  8. ‘He was so frail’: Sierra College coach recalls rise of Aiyuk ...

    www.aol.com/frail-sierra-college-coach-recalls...

    The venue for 17 years was used as San Francisco’s training camp home, starting with its first Super Bowl championship season of 1981 and continuing through each of its five Lombardi Trophy seasons.

  9. CADASIL - Wikipedia

    en.wikipedia.org/wiki/CADASIL

    The mean age of onset of ischemic episodes is approximately 46 years (range 30–70). A classic lacunar syndrome occurs in at least two-thirds of affected patients while hemispheric strokes are much less common. It is worthy of note that ischemic strokes typically occur in the absence of traditional cardiovascular risk factors.