enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Distal 18q- - Wikipedia

    en.wikipedia.org/wiki/Distal_18q-

    Specialty. Medical genetics. Distal 18q- is a genetic condition caused by a deletion of genetic material within one of the two copies of chromosome 18. [1] The deletion involves the distal section of 18q and typically extends to the tip of the long arm of chromosome 18. [2]

  3. Ring chromosome 18 - Wikipedia

    en.wikipedia.org/wiki/Ring_chromosome_18

    Individuals with ring 18 have one of their two copies of chromosome 18 that has formed the shape of a ring. The ring is formed when the caps on both the long arm (q) and the short arm (p) of one copy of chromosome 18 are lost and the new ends re-join to form the ring. Because the ring involves deletions of both the long arm (18q-) and the short ...

  4. Proximal 18q- - Wikipedia

    en.wikipedia.org/wiki/Proximal_18q-

    Proximal 18q-is a rare genetic condition caused by a deletion of genetic material within one of the two copies of chromosome 18. This deletion involves the proximal (near the centromere ) section of the long arm of chromosome 18 somewhere between 18q11.2 (18.9 Mb) to 18q21.1 (43.8 Mb). [1]

  5. Y chromosome microdeletion - Wikipedia

    en.wikipedia.org/wiki/Y_chromosome_microdeletion

    Y chromosome microdeletion. Y chromosome microdeletion (YCM) is a family of genetic disorders caused by missing genes in the Y chromosome. Many men with YCM exhibit no symptoms and lead normal lives. It is present in a significant number of men with reduced fertility. [1] Reduced sperm production varies from oligozoospermia, significant lack of ...

  6. 1q21.1 duplication syndrome - Wikipedia

    en.wikipedia.org/wiki/1q21.1_duplication_syndrome

    1q21.1 duplication syndrome, also known as 1q21.1 microduplication, is an uncommon copy number variant associated with several congenital abnormalities, including developmental delay , dysmorphic traits, autism spectrum disorder , and congenital cardiac defects. [1] Common facial features include frontal bossing, hypertelorism, and macrocephaly.

  7. Why is rheumatoid arthritis tied to a higher risk of ... - AOL

    www.aol.com/why-rheumatoid-arthritis-tied-higher...

    Systemic inflammation caused by rheumatoid arthritis could make cognitive decline more likely. Image credit: Juan Claudio Perez/Getty Images. As of 2020, about 17.6 million people worldwide have ...

  8. XX male syndrome - Wikipedia

    en.wikipedia.org/wiki/XX_male_syndrome

    XX male syndrome, also known as de la Chapelle syndrome, is a rare condition in which an individual with a 46,XX karyotype develops a male phenotype. [2] Synonyms for XX male syndrome include 46,XX testicular difference of sex development (or 46,XX DSD) [3] [4] [5] [6]

  9. 13 sneaky signs your testosterone is too low

    www.aol.com/13-sneaky-signs-testosterone-too...

    1. Low Libido. While medications, relationship struggles, and illness can all make you lose interest in sex, a low sex drive is one of the most common symptoms of low testosterone. A drastic drop ...