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Symptom Checker » Claw hand » Hand symptoms
 

Claw hand and Hand symptoms and Long thin fingers and Skin texture changes and Tooth deformity and Weight symptoms
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Claw hand and Hand symptoms and Long thin fingers and Skin texture changes and Tooth deformity and Weight symptoms

  • Claw hand AND Hand symptoms AND Long thin fingers AND Skin texture changes AND Tooth deformity AND Weight symptoms - Causes of All Symptoms
  • Claw hand OR Hand symptoms OR Long thin fingers OR Skin texture changes OR Tooth deformity OR Weight symptoms - 3877 causes

Claw hand:

Hand symptoms:

Long thin fingers:

Skin texture changes:

Tooth deformity:

Weight symptoms:

Results: Causes of Claw hand AND Hand symptoms AND Long thin fingers AND Skin texture changes AND Tooth deformity AND Weight symptoms

Results: 3877 causes of Claw hand OR Hand symptoms OR Long thin fingers OR Skin texture changes OR Tooth deformity OR Weight symptoms

    1. 14q+ syndrome
     A rare chromosomal disorder involving duplication of genetic material from the long arm (q) of chromosome 14 resulting in various abnormalities....more »
    2. 18p minus syndrome
     A rare chromosomal disorder where a portion of chromosome 18 is missing which is characterized by mental and growth deficiencies, drooping upper eyelid and prominent ears. The type and severity of symptoms is determined by the amount of genetic material t...more »
    3. 1q deletion
     A rare chromosomal disorder where part of the long arm (q) of chromosome 1 is deleted resulting in various abnormalities which are determined by the size of the deleted portion....more »
    4. 1q proximal deletion
     A rare chromosomal disorder where the proximal part of the long arm (q) of chromosome 1 is deleted resulting in various abnormalities....more »
    5. 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 »
    6. 2q deletion
     A rare chromosomal disorder where part of the long arm (q) of chromosome 2 is deleted resulting in various abnormalities which are determined by the size of the deleted portion....more »
    7. 2q22-q24 deletion
     A rare chromosomal disorder where part of the long arm (q22-q24) of chromosome 2 is deleted resulting in various abnormalities which are determined by the size of the deleted portion....more »
    8. 3-Hydroxyisobutyric aciduria
     A rare inborn metabolic disorder which causes brain and facial anomalies, seizures and growth problems....more »
    9. 3-M Syndrome
     A rare genetic condition which is characterized by distinctive physical features and severe growth retardation that starts during the fetal stage. Intelligence is not affected....more »
    10. 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 »

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