X linked Copper Deficiency

It is possible that the major title of the rating Menkes Disease is not the name you anticipated. Please inspect the words listing to locate the alternating name(s) and condition subdivision(s) covered by this report.

Basic synonyms

  • Kinky Hair Disease
  • Steely Hair Disease
  • Trichopoliodystrophy
  • X-linked Copper Deficiency
  • Copper Transport Illness

Condition Communities

  • X-linked Copper Malabsorption
  • Neurodegenerative disease

General Discussion
Menkes disease is a genetic disorder of copper metabolic rate that is noticeable before birth (prenatally) and which follows a gradually degenerative path involving a number of body organs of the body yet specifically the human brain. It is identified by seizures, dementia, stunted development, failure to grow, unpredictable body temperature level, and really unusual shade and also structure of hair.

It is the failing of the copper transport systems within the cell and afterwards throughout the cell membrane layer that accountables for the symptoms of the problem. Due to the failing of this transportation system, copper is unavailable to different cells where it is crucial for the framework as well as feature of numerous enzymes that regulate the advancement of hair, human brain, bones, liver as well as arteries.

Menkes disease is an X-linked genetic disorder dued to anomalies in the ATP7A genetics that accountables for production of the ATPase enzyme that manages copper levels in the body. Versions of Menkes that are caused by mutations in the ATP7A gene but lead to less extreme symptoms consist of light Menkes condition and also occipital horn disorder.

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