Cracked skin and Diarrhea and Mouth infections and Muscle symptoms and Rash and Swallowing symptoms

Cracked skin OR Diarrhea OR Mouth infections OR Muscle symptoms OR Rash OR Swallowing symptoms: 3009 causes

1. 14q+ syndrome
 A rare chromosomal disorder involving duplication of genetic material from the long arm (q) of chromosome 14 resulting in various abnormalities....read 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...read 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....read more »
4. 1q terminal deletion
 A rare chromosomal disorder where the terminal part of the long arm (q) of chromosome 1 is deleted resulting in various abnormalities....read more »
5. 2-Hydroxyglutaricaciduria
 A rare metabolic disorder characterized by high levels of a certain chemical (2-Hydroxyglutaric) which causes a serious progressive neurological disease and damage to the brain. The features of this disorder are variable and some cases are milder than oth...read more »
6. 2-hydroxyethyl methacrylate sensitization
 A condition where exposure to 2-hydroxyethyl methacrylate results in sensitization to the chemical - further exposure to the chemical causes a reaction. The chemical is used in dental work so dental patients and dental workers are at risk of becoming sens...read more »
7. 2-methylbutyryl-coenzyme A dehydrogenase deficiency
 A very rare genetic disorder where an enzyme deficiency prevents the break down of certain proteins into energy and results in a harmful accumulation of acids in the blood and body tissues. More specifically, there is a deficiency of an enzyme (2-methylbu...read more »
8. 2p21 deletion syndrome
 This syndrome is a more severe form hypotonia-cystinuria syndrome as a larger portion of genetic material from chromosome 2p21 is deleted. It is characterized by infant seizures, reduced muscle tone, developmental delay, lactic acidosis and unusual facial...read more »
9. 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....read more »
10. 3 alpha methylcrotonyl-Coa carboxylase 1 deficiency
 A rare inherited disorder where lack of a certain enzyme (3-methylcrotonyl-Coa carboxylase) stops proteins with the amino acid leucine being metabolized normally by the body. The leucine builds up in the body and causes damage to the brain and nervous sys...read more »

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