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  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. Trisomy 18 - Wikipedia

    en.wikipedia.org/wiki/Trisomy_18

    1 per 5,000 births [ 3] Trisomy 18, also known as Edwards syndrome, is a genetic disorder caused by the presence of a third copy of all or part of chromosome 18. [ 3] Many parts of the body are affected. [ 3] Babies are often born small and have heart defects. [ 3] Other features include a small head, small jaw, clenched fists with overlapping ...

  5. Erythromelalgia - Wikipedia

    en.wikipedia.org/wiki/Erythromelalgia

    Erythromelalgia. Erythromelalgia or Mitchell's disease (after Silas Weir Mitchell) is a rare vascular peripheral pain disorder in which blood vessels, usually in the lower extremities or hands, are episodically blocked (frequently on and off daily), then become hyperemic and inflamed. There is severe burning pain (in the small fiber sensory ...

  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. Muscular dystrophy - Wikipedia

    en.wikipedia.org/wiki/Muscular_Dystrophy

    Muscular dystrophies ( MD) are a genetically and clinically heterogeneous group of rare neuromuscular diseases that cause progressive weakness and breakdown of skeletal muscles over time. [ 1] The disorders differ as to which muscles are primarily affected, the degree of weakness, how fast they worsen, and when symptoms begin. [ 1]

  8. Wallerian degeneration - Wikipedia

    en.wikipedia.org/wiki/Wallerian_degeneration

    Wallerian degeneration is an active process of degeneration that results when a nerve fiber is cut or crushed and the part of the axon distal to the injury (which in most cases is farther from the neuron 's cell body) degenerates. [ 1] A related process of dying back or retrograde degeneration known as 'Wallerian-like degeneration' occurs in ...

  9. Brad Pitt Is 'Getting Updates' on Son Pax's Recovery Despite ...

    www.aol.com/lifestyle/brad-pitt-getting-updates...

    Brad Pitt is "getting updates" about son Pax's recovery from an accident despite being estranged from his adult children, a source tells PEOPLE. "He hasn't had any contact with Pax in years, but ...