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Lipodystrophy due to peptidic growth factors deficiency

MONDO:0009312

Deficiency of the peptidic growth factors is characterized by loss of subcutaneous fat layers on the limbs, lipodystrophy in the face and trunk and scleroderma-like skin disorders (thickened skin on the palms and soles and skin pigment changes on the limbs and trunk).

Also known as: Hoepffner-Dreyer-Reimers syndrome, Werner-like syndrome due to combined growth factor deficiency, combined insulin, insulin-like growth factor 1 (IGF1) and epidermal growth factor (EGF) deficiency, Hoepffner Dreyer Reimers syndrome, Werner-like syndrome due to combined Growth Factor deficiency, growth factors, combined defect OF, insulin, insulin-like Growth Factor I, and Epidermal Growth Factor deficiency, peptide growth factors deficiency

34 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Metabolic disease (215) Hereditary disease (172) Skin disorder (123) Inborn errors of metabolism (42) Lipodystrophy (26) Human disease (14) Hereditary skin disorder (5) Disease of genetic or genomic mechanism (2) Hereditary lipodystrophy (2)
Trials to join now! 19 Not yet recruiting 4 Not yet finished but already full! 4 Completed 7
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