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  2. Turner syndrome - Wikipedia

    en.wikipedia.org/wiki/Turner_syndrome

    Turner syndrome (TS), commonly known as 45,X, or 45,XO, [note 1] is a chromosomal disorder in which cells have only one X chromosome or are partially missing an X chromosome (sex chromosome monosomy) leading to the complete or partial deletion of the pseudoautosomal regions (PAR1, PAR2) in the affected X chromosome.

  3. Webbed neck - Wikipedia

    en.wikipedia.org/wiki/Webbed_neck

    It is a feature of Turner syndrome [1] (only found in girls) and Noonan syndrome, [2] as well as the rarer Klippel–Feil syndrome, [3] or Diamond–Blackfan anemia. [ 4 ] References

  4. Noonan syndrome - Wikipedia

    en.wikipedia.org/wiki/Noonan_syndrome

    While Turner syndrome has similarities with renal anomalies and developmental delay, Turner syndrome is only found in females and often expresses differently. In Turner syndrome, there is a lower incidence of developmental delays, left-sided heart defects are constant and the occurrence of renal abnormalities is much lower. [36] Other RASopathies

  5. List of syndromes - Wikipedia

    en.wikipedia.org/wiki/List_of_syndromes

    Wilson–Mikity syndrome; Wilson–Turner syndrome; Winchester syndrome; Winter-over syndrome; Wiskott–Aldrich syndrome; Wissler's syndrome; Withdrawal syndrome; Withering abalone syndrome; Wobbly hedgehog syndrome; Wolcott–Rallison syndrome; Wolff–Parkinson–White syndrome; Wolfram syndrome; Wolf–Hirschhorn syndrome; Woodhouse ...

  6. Parsonage–Turner syndrome - Wikipedia

    en.wikipedia.org/wiki/Parsonage–Turner_syndrome

    Parsonage–Turner syndrome, also known as acute brachial neuropathy, neuralgic amyotrophy and abbreviated PTS, is a syndrome of unknown cause; although many specific risk factors have been identified (such as; post-operative, post-infectious, post-traumatic or post-vaccination). [4]

  7. Gonadal dysgenesis - Wikipedia

    en.wikipedia.org/wiki/Gonadal_dysgenesis

    Turner syndrome is usually not diagnosed until a delayed onset of puberty with Müllerian structures found to be in infantile stage. [4] Physical phenotypic characteristics include short stature, dysmorphic features and lymphedema at birth. [23] Comorbidities include heart defects, vision and hearing problems, diabetes, and low thyroid hormone ...

  8. After Dad's Cancer Diagnosis, a Family Had Their Stomachs ...

    www.aol.com/lifestyle/dads-cancer-diagnosis...

    Kristie and Greg regularly send each other Instagram recipes and beautiful food pictures. Now, Kori explains, the family front-loads meals with protein. Carbs and sugars are hard for them to process.

  9. Henry Turner (endocrinologist) - Wikipedia

    en.wikipedia.org/wiki/Henry_Turner_(endocrinologist)

    Henry Hubert Turner (August 28, 1892 – August 4, 1970) was an American endocrinologist, noted for his published description of Turner syndrome in 1938 at the annual meeting of the Association for the Study of Internal Secretions.