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  2. 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.

  3. Dunnigan familial partial lipodystrophy - Wikipedia

    en.wikipedia.org/wiki/Dunnigan_familial_partial...

    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 ...

  4. Lipodystrophy - Wikipedia

    en.wikipedia.org/wiki/Lipodystrophy

    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 .

  5. Category:Lipid metabolism disorders - Wikipedia

    en.wikipedia.org/wiki/Category:Lipid_metabolism...

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file

  6. Lupinranger VS Patranger VS Kyuranger - Wikipedia

    en.wikipedia.org/wiki/Lupinranger_VS_Patranger...

    Concurrently, Kyuranger members Stinger, Hammie, and Spada search for Lucky, but track Minato's guitar to a warehouse, where the Lupinrangers and BN thieves learn that Lipig is working with Don Arkage, who intends to use the Hyper Planedium in Minato's guitar to become invincible. The Lupinrangers and Kyurangers confront the two and defeat ...

  7. Acquired generalized lipodystrophy - Wikipedia

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

    Acquired generalized lipodystrophy (AGL), also known as Lawrence syndrome [1] and Lawrence–Seip syndrome, [1] is a rare skin condition that appears during childhood or adolescence, characterized by fat loss affecting large areas of the body, particularly the face, arms, and legs.

  8. Barraquer–Simons syndrome - Wikipedia

    en.wikipedia.org/wiki/Barraquer–Simons_syndrome

    A genetic workup should be performed if the familial form of lipodystrophy is suggested. Laboratory work for associated diseases includes: [ citation needed ] Metabolic disease - fasting glucose, glucose tolerance test, lipid profile, and fasting insulin to characterize the insulin resistance state; free testosterone (in women) to look for ...

  9. Congenital generalized lipodystrophy - Wikipedia

    en.wikipedia.org/wiki/Congenital_generalized...

    Congenital generalized lipodystrophy (also known as Berardinelli–Seip lipodystrophy) is an extremely rare autosomal recessive condition, characterized by an extreme scarcity of fat in the subcutaneous tissues. [2] It is a type of lipodystrophy disorder where the magnitude of fat loss determines the severity of metabolic complications. [3]