Page last updated: 2024-11-04

carbamylhydrazine and Menkes Kinky Hair Syndrome

carbamylhydrazine has been researched along with Menkes Kinky Hair Syndrome in 1 studies

carbamylhydrazine: RN given refers to parent cpd

Menkes Kinky Hair Syndrome: An inherited disorder of copper metabolism transmitted as an X-linked trait and characterized by the infantile onset of HYPOTHERMIA, feeding difficulties, hypotonia, SEIZURES, bony deformities, pili torti (twisted hair), and severely impaired intellectual development. Defective copper transport across plasma and endoplasmic reticulum membranes results in copper being unavailable for the synthesis of several copper containing enzymes, including PROTEIN-LYSINE 6-OXIDASE; CERULOPLASMIN; and SUPEROXIDE DISMUTASE. Pathologic changes include defects in arterial elastin, neuronal loss, and gliosis. (From Menkes, Textbook of Child Neurology, 5th ed, p125)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hartmann, C1
McIntire, WS1

Other Studies

1 other study available for carbamylhydrazine and Menkes Kinky Hair Syndrome

ArticleYear
Amine-oxidizing quinoproteins.
    Methods in enzymology, 1997, Volume: 280

    Topics: Amino Acid Sequence; Coenzymes; Copper; Diabetes Mellitus; Dihydroxyphenylalanine; Electron Spin Res

1997