When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Turner syndrome - Wikipedia

    en.wikipedia.org/wiki/Turner_syndrome

    Turner syndrome (TS), commonly known as 45,X, or 45,X0, [note 1] is a chromosomal disorder in which female cells have only one X chromosome instead of two, 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. 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]

  4. Henry Turner (endocrinologist) - Wikipedia

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

    Children 2 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.

  5. 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 ...

  6. Ullrich congenital muscular dystrophy - Wikipedia

    en.wikipedia.org/wiki/Ullrich_congenital...

    Ullrich congenital muscular dystrophy (UCMD) is a form of congenital muscular dystrophy.There are two forms: UCMD1 and UCMD2. [4]UCMD1 is associated with variants of type VI collagen, while UCMD2 is associated with variants of type XII collagen.

  7. Guillain-Barre syndrome had 3-year-old son of Dodgers ...

    www.aol.com/lifestyle/guillan-barre-syndrome-had...

    Max “rapidly declined and went into full-body paralysis,” wrote Chelsea in an Aug. 2 post. The 3-year-old spent several days on a ventilator to support his lung function.

  8. Final Photo Captures Grandparents Trapped On Roof Before ...

    www.aol.com/heartbreaking-final-photo-shows...

    A final photo has emerged of North Carolina grandparents on the roof of their home, surrounded by floodwaters, minutes before they drowned due to Hurricane Helene. Jessica Drye Turner’s family ...

  9. Cubitus valgus - Wikipedia

    en.wikipedia.org/wiki/Cubitus_valgus

    Cubitus valgus is a medical deformity in which the forearm is angled away from the body to a greater degree than normal when fully extended. A small degree of cubitus valgus (known as the carrying angle) is acceptable and occurs in the general population.