Naslov
S-Adenosylhomocysteine hydrolase deficiency in a 26-year-old man

Autori
Buist, Neil R.M. ; Glenn, Byron ; Vugrek, Oliver ; Wagner, Conrad ; Stabler, Sally ; Allen, Robert H. ; Pogribny, Igor ; Schulze, Andreas ; Zeisel, Steven H. ; Barić, Ivo ; Mudd, Harvey S.

Izvornik
Journal of Inherited Metabolic Diseaseas (0141-8955) 29 (2006), 4; 538-545

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
methionine; S-adenosylhomocysteine hydrolase deficiency; S-adenosylmethionine; hypermethioninemia; myopathy

Sažetak
This paper reports the third proven human case of deficient S-adenosylhomocysteine (AdoHcy) hydrolase activity. The patient is similar to the only two previously reported cases with this disorder in having severe myopathy, developmental delay, elevated serum creatine kinase (CK) concentrations, and hypermethioninemia. Although he has been followed from infancy, the basic enzyme deficiency was established only at age 26 years. The diagnosis was based on markedly elevated plasma concentrations of both AdoHcy and S-adenosylmethionine, some 20 % of the mean control activity of AdoHcy hydrolase activity in hemolysates of his red-blood cells and two missense mutations in his gene encoding AdoHcy hydrolase. He had low values of erythrocyte phosphatidylcholine and plasma fee choline and marginally elevated excretion of guanidinoacetate, suggesting that the elevated AdoHcy may have been inhibiting methylation of phosphatidylethanolamine and guanidinoacetate. His leucocyte DNA was globally more methylated than the DNA's of his parents or the mean extent of methylation measured in age-matched control subjects

Izvorni jezik
Engleski

Znanstvena područja
Biologija, Temeljne medicinske znanosti, Kliničke medicinske znanosti

POVEZANOST RADA