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Familial Partial Lipodystrophy, Dunnigan Type Autosomal dominant is the manner of inheritance of this condition Dunnigan-type familial partial lipodystrophy , also known as FPLD Type II and abbreviated as ( FPLD2 ), is a rare monogenic form of insulin resistance characterized by loss of subcutaneous fat from the extremities , trunk , and ...
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.
Barraquer–Simons syndrome is a rare form of lipodystrophy, which usually first affects the head, and then spreads to the thorax. [ 2 ] [ 3 ] It is named for Luis Barraquer Roviralta (1855–1928), a Spanish physician, and Arthur Simons (1879–1942), a German physician.
Drug-induced lipodystrophy; Dunnigan familial partial lipodystrophy; E. ... Marfanoid–progeroid–lipodystrophy syndrome; N. Neutrophilic lobular panniculitis;
Upon comparing pictures of partial lipodystrophy patients, Viles speculated that she might be affected by both partial lipodystrophy and Emery-Dreifuss muscular dystrophy. [ 11 ] [ 4 ] She attended a medical conference at Hopkins where she showed photos to doctors and informed them of her belief that she had not one, but two, rare genetic ...
Lipodystrophy syndromes are a group of genetic or acquired disorders in which the body is unable to produce and maintain healthy fat tissue. [1] [2] The medical condition is characterized by abnormal or degenerative conditions of the body's adipose tissue.
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Lipodystrophy: Familial partial lipodystrophy (Köbberling–Dunnigan syndrome) Calf muscle /general [50] [7] Adolescence-onset Hypertrophy of calf muscles [50] [7] Congenital generalized lipodystrophy (Berardinelli–Seip syndrome) General [8] Infantile-onset Muscle hypertrophy [8] Hypertonia (spasticity or rigidity) Spastic cerebral palsy ...