enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Lipodystrophy - Wikipedia

    en.wikipedia.org/wiki/Lipodystrophy

    The medicine is used in: adults and children above the age of two years with generalised lipodystrophy (Berardinelli-Seip syndrome and Lawrence syndrome) and in adults and children above the age of 12 years with partial lipodystrophy (including Barraquer-Simons syndrome), when standard treatments have failed.

  3. MDP syndrome - Wikipedia

    en.wikipedia.org/wiki/MDP_syndrome

    MDP syndrome, also known as mandibular dysplasia with deafness and progeroid features, is an extremely rare metabolic disorder that prevents fatty tissue from being stored underneath the skin. It is only known to affect a very small number of people worldwide (fewer than 12 cases have been diagnosed as of December 2014).

  4. CANDLE syndrome - Wikipedia

    en.wikipedia.org/wiki/CANDLE_syndrome

    Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature (CANDLE) syndrome is an autosomal recessive disorder that presents itself via various autoinflammatory responses throughout the body, multiple types of skin lesions, and recurrent long-term fever symptoms. [1]

  5. Acquired generalized lipodystrophy - Wikipedia

    en.wikipedia.org/wiki/Acquired_generalized...

    The clinical presentation is similar to people with congenital lipodystrophy: the only difference is that AGL patients are born with normal fat distribution and symptoms develop in childhood and adolescence years and rarely begins after 30 years of age. [6] [7] Females are more often affected than males, with ratio being 3:1. [5] [6] [8] [page ...

  6. Werner syndrome - Wikipedia

    en.wikipedia.org/wiki/Werner_syndrome

    Werner syndrome patients exhibit growth retardation, short stature, premature graying of hair, alopecia (hair loss), wrinkling, prematurely aged faces with beaked noses, skin atrophy (wasting away) with scleroderma-like lesions, lipodystrophy (loss of fat tissues), abnormal fat deposition leading to thin legs and arms, and severe ulcerations around the Achilles tendon and malleoli (around ankles).

  7. Familial partial lipodystrophy - Wikipedia

    en.wikipedia.org/wiki/Familial_partial_lipodystrophy

    Familial partial lipodystrophy, also known as Köbberling–Dunnigan syndrome, [2] is a rare genetic metabolic condition characterized by the loss of subcutaneous fat. [ 3 ] : 495 FPL also refers to a rare metabolic condition in which there is a loss of subcutaneous fat in the arms, legs and lower torso.

  8. Barraquer–Simons syndrome - Wikipedia

    en.wikipedia.org/wiki/Barraquer–Simons_syndrome

    The disease may gradually progress. About 40-50% of patients develop end-stage renal disease over the course of 10 years. This condition is responsible for most recurrent hospital admissions in patients with acquired partial lipodystrophy. Rapid progression of renal disease in a pregnant patient was reported.

  9. Localized lipodystrophy - Wikipedia

    en.wikipedia.org/wiki/Localized_lipodystrophy

    Localized lipodystrophy is a skin condition characterized by the loss of subcutaneous fat localized to sites of insulin injection. [1]: 497 ...