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Acne and Blood symptoms and Deepening voice and Hyperpigmentation in children
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Acne and Blood symptoms and Deepening voice and Hyperpigmentation in children

  • Acne AND Blood symptoms AND Deepening voice AND Hyperpigmentation in children - Causes of All Symptoms
  • Acne OR Blood symptoms OR Deepening voice OR Hyperpigmentation in children - 2313 causes

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Results: Causes of Acne AND Blood symptoms AND Deepening voice AND Hyperpigmentation in children

Note: Do not use for diagnosis; see limitations of results.

Results: 2313 causes of Acne OR Blood symptoms OR Deepening voice OR Hyperpigmentation in children

    1. 22q11.2 deletion syndrome
     A rare genetic disorder caused by the absence of a small portion of genetic material. A small section of chromosome 22 is missing at a location called q11.2. Chromosome 22 is one of 23 pairs of chromosomes that exist in humans....more »
    2. 3-Hydroxyacyl-CoA Dehydrogenase II Deficiency
     A rare genetic disorder involving the deficiency of an enzyme (hydroxyacyl-coa dehydrogenase). The severity of the symptoms is highly variable with some cases resulting in death during the first decade while others suffer psychomotor and regression. Sympt...more »
    3. 3-alpha-Hydroxyacyl-CoA Dehydrogenase Deficiency
     A rare inherited form of biochemical disorder characterized by the deficiency of a particular enzyme (3-Hydroxyacyl-CoA Dehydrogenase). The enzyme deficiency only affects certain body tissues, in particular the skeletal muscles. The lack of enzyme activit...more »
    4. 3-alpha-hydroxyacyl-coenzyme A dehydrogenase deficiency
     A rare inherited form of biochemical disorder characterized by the deficiency of a particular enzyme (3-Hydroxyacyl-CoA Dehydrogenase). The enzyme deficiency only affects certain body tissues, in particular the skeletal muscles. The lack of enzyme activit...more »
    5. 3-alpha-hydroxyisobutyryl-CoA hydrolase deficiency
     A metabolic disorder involving an enzyme deficiency which causes symptoms such as degeneration of the nervous system. The other features of the disorder are somewhat variable....more »
    6. 3-methylglutaconic aciduria, type 1
     A recessively inherited metabolic disorder characterized by methylglutaconic acid in the urine....more »
    7. 3-methylglutaconic aciduria, type 4
     A rare genetic disorder where the body's cells are unable to make sufficient energy resulting in an accumulation in the body of 3-methylglutaconic acid. Type 4 is characterized by symptoms which overlap type 1 and 3....more »
    8. 3?-hydroxysteroid dehydrogenase deficiency
     A ver rare form of congenital adrenal hyperplasia involving a deficiency of 3?-hydroxysteroid dehydrogenase which results in reduced production of adrenal steroids (mineralocorticoids, sex steroids and glucocorticoids). The disorder can occur in classical...more »
    9. 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency
     A very rare metabolic disorder where a deficiency of a particular enzyme results in the urinary excretion of a chemical called hawkinsin. Symptoms start once the infant is weaned off breast milk....more »
    10. Aase-Smith I syndrome
     A very rare hereditary syndrome characterized by deformities such as joint contractures, anemia, hydrocephalus and cleft palate....more »

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  • Warning - Beta version - information may be incorrect (details)
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