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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.
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 gluteal region.
Drug-induced lipodystrophy; Dunnigan familial partial lipodystrophy; E. ... Marfanoid–progeroid–lipodystrophy syndrome; N. Neutrophilic lobular panniculitis;
Both genetic (e.g., Berardinelli-Seip congenital lipodystrophy, Dunnigan familial partial lipodystrophy) and acquired (e.g., HIV-related lipodystrophy in people treated with highly active antiretroviral therapy) forms of lipodystrophy may give rise to severe insulin resistance and many of metabolic syndrome's components. [36]
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 ...
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.
Familial partial lipodystrophy of the Dunnigan type (FPLD) 151660: Lipoatrophic diabetes: Lamin A/C: 2002 [32] Greenberg dysplasia: 215140: Skeletal dysplasia: Lamin B receptor: 2003 [33] Hutchinson–Gilford progeria syndrome (HGPS) 176670: Progeria: Lamin A/C: 2003 [17] Leukodystrophy, demyelinating, adult-onset, autosomal dominant (ADLD) 169500
Short rib–polydactyly syndrome is a family of four closely related dysplasias: I – "Saldino-Noonan type" II – "Majewski type"