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Wilson's disease--in a 2 year old child. 1979

C T Lim, and K E Choo

UI MeSH Term Description Entries
D008297 Male Males
D002675 Child, Preschool A child between the ages of 2 and 5. Children, Preschool,Preschool Child,Preschool Children
D006527 Hepatolenticular Degeneration A rare autosomal recessive disease characterized by the deposition of copper in the BRAIN; LIVER; CORNEA; and other organs. It is caused by defects in the ATP7B gene encoding copper-transporting ATPase 2 (EC 3.6.3.4), also known as the Wilson disease protein. The overload of copper inevitably leads to progressive liver and neurological dysfunction such as LIVER CIRRHOSIS; TREMOR; ATAXIA and intellectual deterioration. Hepatic dysfunction may precede neurologic dysfunction by several years. Cerebral Pseudosclerosis,Neurohepatic Degeneration,Pseudosclerosis,Wilson Disease,Copper Storage Disease,Hepatic Form of Wilson Disease,Hepato-Neurologic Wilson Disease,Hepatocerebral Degeneration,Hepatolenticular Degeneration Syndrome,Kinnier-Wilson Disease,Progressive Lenticular Degeneration,Westphal-Strumpell Syndrome,Wilson Disease, Hepatic Form,Wilson's Disease,Cerebral Pseudoscleroses,Copper Storage Diseases,Degeneration Syndrome, Hepatolenticular,Degeneration Syndromes, Hepatolenticular,Degeneration, Hepatocerebral,Degeneration, Hepatolenticular,Degeneration, Neurohepatic,Degeneration, Progressive Lenticular,Degenerations, Hepatocerebral,Degenerations, Neurohepatic,Disease, Copper Storage,Diseases, Copper Storage,Diseases, Hepato-Neurologic Wilson,Diseases, Kinnier-Wilson,Hepato Neurologic Wilson Disease,Hepato-Neurologic Wilson Diseases,Hepatocerebral Degenerations,Hepatolenticular Degeneration Syndromes,Kinnier Wilson Disease,Kinnier-Wilson Diseases,Lenticular Degeneration, Progressive,Neurohepatic Degenerations,Pseudoscleroses, Cerebral,Pseudosclerosis, Cerebral,Storage Disease, Copper,Storage Diseases, Copper,Syndrome, Hepatolenticular Degeneration,Syndromes, Hepatolenticular Degeneration,Westphal Strumpell Syndrome,Westphal-Strumpell Syndromes,Wilson Disease, Hepato-Neurologic,Wilson Diseases, Hepato-Neurologic,Wilsons Disease
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

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C T Lim, and K E Choo
Diagnosing Wilson's disease in a 5-year-old child.
August 2002, Journal of paediatrics and child health,
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[Castleman's disease in a 2-year-old child].
April 1988, Anales espanoles de pediatria,
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[Hirschsprung disease in a 2-year-old child].
January 1953, Revista portuguesa de medicina militar,
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Perthes disease in a 2-year-old child.
March 2015, BMJ case reports,
C T Lim, and K E Choo
[Rheumatic disease in a 2 year old child].
May 1951, Revista chilena de pediatria,
C T Lim, and K E Choo
[Wilson's disease with preceding hepatic and hematological symptoms in a 10-year-old child].
February 1963, Archives francaises de pediatrie,
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[Papillon-Lefevre disease in a 2 1/2-year-old child].
March 1975, Pediatriia,
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Diffuse pulmonary disease in a 2 1/2-year-old child.
August 1982, JAMA,
C T Lim, and K E Choo
[Hand-Schueller-Christian disease in a 2-year-old child].
October 1961, Srpski arhiv za celokupno lekarstvo,
C T Lim, and K E Choo
A typical picture of Kayser-Fleisher ring in an 8-year-old child with Wilson's disease.
January 2023, The Pan African medical journal,
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