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What questions will my doctor ask me once I'm diagnosed with inherited lipodystrophy?

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Your doctor might ask you these questions:

  • What symptoms have you noticed?
  • When did you first see them?
  • Are changes in how your child looks only in certain areas, or all over?
  • Have you had his blood sugar, cholesterol, and triglyceride levels checked?
  • Has he had bad belly aches or oily poop?
  • What other health problems does he have?
  • Are his parents related by blood?
  • Does anyone else in the family have problems with body fat?

From: Inherited Lipodystrophy WebMD Medical Reference

SOURCES:

NORD Physician Guides: "Lipodystrophy Disorders."

FDA: "FDA approves Myalept to treat rare metabolic disease."

Lipodystrophy United: "About Lipodystrophy."

University of Texas Southwestern Medical Center: "Lipodystrophy," "Lipodystrophy Therapies."

Genetics Home Reference: "Berardinelli-Seip congenital lipodystrophy."

KidsHealth: "Acanthosis Nigricans."

AACE Lipodystrophy Detection Consensus Statement, , January-February 2013. Endocrine Practice

Endocrine Society, Resource Room Slide Series: "Lipodystrophy: Metabolic and Clinical Aspects."

DermNet NZ: "Lipodystrophy."

Orphanet: "Berardinelli-Seip congenital lipodystrophy," "Familial partial lipodystrophy, Köbberling type," "Familial partial lipodystrophy, Dunnigan type," "Familial partial lipodystrophy associated with PPARG mutations."

Reviewed by Jennifer Robinson on February 2, 2019

SOURCES:

NORD Physician Guides: "Lipodystrophy Disorders."

FDA: "FDA approves Myalept to treat rare metabolic disease."

Lipodystrophy United: "About Lipodystrophy."

University of Texas Southwestern Medical Center: "Lipodystrophy," "Lipodystrophy Therapies."

Genetics Home Reference: "Berardinelli-Seip congenital lipodystrophy."

KidsHealth: "Acanthosis Nigricans."

AACE Lipodystrophy Detection Consensus Statement, , January-February 2013. Endocrine Practice

Endocrine Society, Resource Room Slide Series: "Lipodystrophy: Metabolic and Clinical Aspects."

DermNet NZ: "Lipodystrophy."

Orphanet: "Berardinelli-Seip congenital lipodystrophy," "Familial partial lipodystrophy, Köbberling type," "Familial partial lipodystrophy, Dunnigan type," "Familial partial lipodystrophy associated with PPARG mutations."

Reviewed by Jennifer Robinson on February 2, 2019

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Is family history important when diagnosis inherited lipodystrophy?

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