Rationale: On account of the diversity and rarity of lipodystrophy, this condition may be frequently unrecognized or misdiagnosed. This tends to be concerning as it is progressive and has potentially life-threatening complications. Patient Concerns: The patient was referred to our clinic with chief complaints of uncontrolled glycemia and an increased frequency of urination since last 3 months. The patient complained of weakness that led to thinning of upper limb muscles, loss of fat from face, neck, and upper thorax with simultaneous increase in abdominal girth, flattening of buttocks, and reduction in girth of lower limb muscles. Diagnosis: The patient was diagnosed with partial lipodystrophy of limbs (PLL) based on unique clinical feature...
Purpose/Aim of the study: Acquired partial lipodystrophy (APL) is a rare disease characterized by se...
Lipodystrophy is regarded as a functional disturbance of the hypothalamus. Typically, face is the fi...
Background: Dunnigan-type familial partial lipodystrophy (FPLD2) is a rare autosomal dominant diseas...
WOS: 000380079700009PubMed ID: 26776282Objective: Partial lipodystrophy of the limbs (PLL) is a newl...
OBJECTIVEdLipodystrophies are categorized by the extent of fat loss (generalized vs. partial) and by...
International audienceBACKGROUND: Lipodystrophic syndromes are rare diseases of genetic or acquired ...
Purpose/Aim of the study: Acquired partial lipodystrophy (APL) is a rare disease characterized by se...
PubMed ID: 26139569Objective Acquired partial lipodystrophy (APL) is a rare disorder characterized b...
Lipodystrophies are a genetically heterogeneous group of disorders characterized by loss of subcutan...
Background: Familial partial lipodystrophies are rare monogenic disorders that are often associated ...
Context: Lipodystrophy syndromes are a heterogeneous group of rare genetic or acquired disorders cha...
Lipodystrophy syndromes are rare heterogeneous disorders characterized by deficiency of adipose tiss...
International audienceLipodystrophic syndromes are acquired or genetic rare diseases, characterised ...
Introduction: Lipodystrophy is a heterogeneous group of rare diseases characterized by various degre...
Metabolic studies were performed in three patients with partial lipodystrophy. These studies demonst...
Purpose/Aim of the study: Acquired partial lipodystrophy (APL) is a rare disease characterized by se...
Lipodystrophy is regarded as a functional disturbance of the hypothalamus. Typically, face is the fi...
Background: Dunnigan-type familial partial lipodystrophy (FPLD2) is a rare autosomal dominant diseas...
WOS: 000380079700009PubMed ID: 26776282Objective: Partial lipodystrophy of the limbs (PLL) is a newl...
OBJECTIVEdLipodystrophies are categorized by the extent of fat loss (generalized vs. partial) and by...
International audienceBACKGROUND: Lipodystrophic syndromes are rare diseases of genetic or acquired ...
Purpose/Aim of the study: Acquired partial lipodystrophy (APL) is a rare disease characterized by se...
PubMed ID: 26139569Objective Acquired partial lipodystrophy (APL) is a rare disorder characterized b...
Lipodystrophies are a genetically heterogeneous group of disorders characterized by loss of subcutan...
Background: Familial partial lipodystrophies are rare monogenic disorders that are often associated ...
Context: Lipodystrophy syndromes are a heterogeneous group of rare genetic or acquired disorders cha...
Lipodystrophy syndromes are rare heterogeneous disorders characterized by deficiency of adipose tiss...
International audienceLipodystrophic syndromes are acquired or genetic rare diseases, characterised ...
Introduction: Lipodystrophy is a heterogeneous group of rare diseases characterized by various degre...
Metabolic studies were performed in three patients with partial lipodystrophy. These studies demonst...
Purpose/Aim of the study: Acquired partial lipodystrophy (APL) is a rare disease characterized by se...
Lipodystrophy is regarded as a functional disturbance of the hypothalamus. Typically, face is the fi...
Background: Dunnigan-type familial partial lipodystrophy (FPLD2) is a rare autosomal dominant diseas...