- progressive partial lipodystrophy
- partial l.
Medical dictionary. 2011.
Medical dictionary. 2011.
partial lipodystrophy — a condition usually seen in girls younger than age 10, characterized by a symmetrical loss of subcutaneous fat, generally beginning on the face and gradually extending to the chest, neck, back, and upper extremities, giving the lower part of the… … Medical dictionary
Lipodystrophy — A disorder of adipose (fatty) tissue characterized by a selective loss of body fat. Patients with lipodystrophy have a tendency to develop insulin resistance, diabetes, a high triglyceride level (hypertriglyceridemia), and fatty liver. There are… … Medical dictionary
progressive lipodystrophy — partial l … Medical dictionary
Congenital generalized lipodystrophy — Classification and external resources eMedicine article/1113171 Congenital generalized lipodystrophy (also known as Berardinelli–Seip syndrome) is a rare autosomal dominant skin condition, characterized by an extreme paucity of fat in the… … Wikipedia
Barraquer–Simons syndrome — Barraquer Simons syndrome Classification and external resources ICD 10 272.6 OMIM 608709 DiseasesDB … Wikipedia
List of cutaneous conditions — This is an incomplete list, which may never be able to satisfy particular standards for completeness. You can help by expanding it with reliably sourced entries. See also: Cutaneous conditions, Category:Cutaneous conditions, and ICD 10… … Wikipedia
syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… … Medical dictionary
Laminopathy — Normal nuclear lamina (a and b) and mutant nuclear lamina (c and d) from a patient with HGPS, visualized by immunofluorescence note the irregular and bumpy shape of the laminopathic nuclei[1] Laminopathies are a group of rare genetic disorders… … Wikipedia
Ohtahara syndrome — Classification and external resources ICD 10 G40.4 OMIM 308350 DiseasesDB … Wikipedia
Charcot–Marie–Tooth disease — Charcot Marie Tooth disease Classification and external resources The foot of a person with Charcot Marie Tooth. The lack of muscle, a high arch, and claw toes are signs of the genetic disease. ICD 10 … Wikipedia