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- Disease Information
- Disease Comparison
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Disease Processes ▼
- Auto Immune
- Vascular-Arteriosclerosis
- Biochemical
- Congenital-developmental
- Deficiency
- Degenrative-Necrosis
- Electromagnetic-Physics
- Eponymic
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- Idiopathic
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- Infectious agent
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- Trauma
- Use-age-Atrophic
- Endocrine-Vegetative
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Major Organs-Systems ▼
- Systemic
- Pediatric
- Nervous & Sensory System (Neurology)
- Cardiovascular System
- Respiratory (Pulmonary) System
- Gastro-Intestinal (Digestive) System
- Urinary System
- Dermatologic System
- Endocrine System
- Immune System
- Musculoskeletal System
- Genital Reproductive System
- Hematopoietic System (Hematology)
- Lymphatic System
- Tissue/Cells/Organelles
Disease Information for Lipodystrophy/familial/dominant
- Clinical Manifestations
- Signs & Symptoms
- Adolescent
- Cheeks Sunken/Wasting
- High blood pressure child
- Atrophic subcutaneous/fatty deposits signs
- Loss of body fat/trunk/limbs
- Xanthomata
- Facial muscle weakness/myopathy
- Labia hypertrophy/female
- Pancreatic symptoms/signs
- Tall child
- Tall Adult
- Clinical Presentation & Variations
- Presentation/Pancreatitis Kids Recurrent
- Disease Progression
- Onset/Adolescence/puberty
- Demographics & Risk Factors
- Population Group
- Child
- Population/Pediatrics population
- Family History
- Family history/Parental consanguinity
- Sex & Age Groups
- Population/Adolescent
- Population/Child
- Population/Children/all
- Population/Female
- Laboratory Tests
- Abnormal Lab Findings (Non Measured)
- Serum lipids increased (Lab)
- Abnormal Lab Findings - Increased
- Glucagon (Lab)
- Glucose, blood (Lab)
- Insulin C-Peptide type, serum (Lab)
- Insulin level (Lab)
- Postprandial Glucose
- Triglycerides (Lab)
- Diagnostic Test Results
- Other Tests & Procedures
- TEST/Glucose intolerance/GTT abnormal
- Pathology
- BX/Abdominal Fat-Pad tissue biopsy/abnormal
- BX/Adipose tissue biopsy/abnormal
- Associated Diseases & Rule outs
- Associated Disease & Complications
- Acanthosis nigricans
- Diabetes mellitus
- Glucose intolerance
- Hyperglycemia
- Hyperlipidemia
- Hypertriglyceridemia
- Insulin resistance
- Lipodystrophy, familial/dominant
- Pancreatitis, acute
- Polycystic ovary/Stein-Leventhal syndrome
- Rieger anomaly/eye
- Disease Mechanism & Classification
- Class
- CLASS/Pediatric disorders (ex)
- CLASS/Adipose tissue disorder (ex).
- CLASS/Fatty tissue/subcutaneous disorder (ex)
- CLASS/Subcutaneous/Panniculus tissue disorder
- Pathophysiology
- Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
- Pathophysiology/Hereditary disease/Adult manifestations
- Pathophysiology/Adipose/Absent triglycerides/fat cells
- Pathophysiology/Subcutaneous manifestation/involvement
- Pathophysiology/Insulin resistant states
- Process
- PROCESS/Atrophic disorders (ex)
- PROCESS/Autosomal dominant hereditary disease (ex).
- PROCESS/Dystrophic disorder (ex)
- PROCESS/INCIDENCE/Rare disease (ex)
- PROCESS/Lipodystrophy disorder (ex)
- Definition
- Be the first to add a definition for Lipodystrophy/familial/dominant
- External Links Related to Lipodystrophy/familial/dominant
- Wikipedia
- Merck
- Images
- PubMed (National Library of Medicine)
- NGC (National Guideline Clearinghouse)
- Medscape (eMedicine)
- Harrison's Online (accessmedicine)
- NEJM (The New England Journal of Medicine)