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Pregled bibliografske jedinice broj: 212646

S-Adenosylhomocysteine hydrolase deficiency: a second patient, the younger brother of the index patient, and outcomes during therapy


Barić, Ivo; Ćuk, Mario; Fumić, Ksenija; Vugrek, Oliver; Allen, R.H.; Glenn, Byron; Maradin, Miljenka; Pažanin, Leo; Pogribny, Igor; Radoš, Marko et al.
S-Adenosylhomocysteine hydrolase deficiency: a second patient, the younger brother of the index patient, and outcomes during therapy // Journal of Inherited Metabolic Disease, 28 (2005), 6; 885-902 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 212646 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
S-Adenosylhomocysteine hydrolase deficiency: a second patient, the younger brother of the index patient, and outcomes during therapy
(S-Adenosylhomocysteine hydrolase deficiency: a second patient, the younger brother of the index patient, and outcomes during therapy.)

Autori
Barić, Ivo ; Ćuk, Mario ; Fumić, Ksenija ; Vugrek, Oliver ; Allen, R.H. ; Glenn, Byron ; Maradin, Miljenka ; Pažanin, Leo ; Pogribny, Igor ; Radoš, Marko ; Sarnavka, Vladimir ; Schulze, Andreas ; Stabler, Sally ; Wagner, Conrad ; Zeisel, Steven H. ; Mudd, Harvey

Izvornik
Journal of Inherited Metabolic Disease (0141-8955) 28 (2005), 6; 885-902

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

Ključne riječi
S-adenosylhomocysteine hydrolase deficiency; treatment

Sažetak
S-Adenosylhomocysteine (AdoHcy) hydrolase deficiency has been proven in a human only once, in a recently described Croatian boy. Here we report the clinical course and biochemical abnormalities of the younger brother of this proband. This younger brother has the same two mutations in the gene encoding AdoHcy hydrolase, and has been monitored since birth. We report, as well, outcomes during therapy for both patients. The information obtained suggests that the disease starts in utero and is characterized primarily by neuromuscular symptomatology (hypotonia, sluggishness, psychomotor delay, absent tendon reflexes, delayed myelination). The laboratory abnormalities are markedly increased creatine kinase and elevated aminotransferases, as well as specific amino acid aberrations that pinpoint the etiology. The latter include, most importantly, markedly elevated plasma AdoHcy. Plasma S-adenosylmethionine (AdoMet) is also elevated, as is methionine (although the hypermethioninemia may be absent or non-significant in the first weeks of life). The disease seems to be at least to some extent treatable, as shown by improved myelination and psychomotor development during dietary methionine restriction and supplementation with creatine and phosphatidylcholine.

Izvorni jezik
Engleski

Znanstvena područja
Kliničke medicinske znanosti



POVEZANOST RADA


Projekti:
0108016
0098086

Ustanove:
Institut "Ruđer Bošković", Zagreb,
Medicinski fakultet, Zagreb,
Klinički bolnički centar Zagreb

Profili:

Avatar Url Marko Radoš (autor)

Avatar Url Ivo Barić (autor)

Avatar Url Leo Pažanin (autor)

Avatar Url Miljenka Maradin (autor)

Avatar Url Oliver Vugrek (autor)

Avatar Url Vladimir Sarnavka (autor)

Avatar Url Mario Ćuk (autor)


Citiraj ovu publikaciju:

Barić, Ivo; Ćuk, Mario; Fumić, Ksenija; Vugrek, Oliver; Allen, R.H.; Glenn, Byron; Maradin, Miljenka; Pažanin, Leo; Pogribny, Igor; Radoš, Marko et al.
S-Adenosylhomocysteine hydrolase deficiency: a second patient, the younger brother of the index patient, and outcomes during therapy // Journal of Inherited Metabolic Disease, 28 (2005), 6; 885-902 (međunarodna recenzija, članak, znanstveni)
Barić, I., Ćuk, M., Fumić, K., Vugrek, O., Allen, R., Glenn, B., Maradin, M., Pažanin, L., Pogribny, I. & Radoš, M. (2005) S-Adenosylhomocysteine hydrolase deficiency: a second patient, the younger brother of the index patient, and outcomes during therapy. Journal of Inherited Metabolic Disease, 28 (6), 885-902.
@article{article, author = {Bari\'{c}, Ivo and \'{C}uk, Mario and Fumi\'{c}, Ksenija and Vugrek, Oliver and Allen, R.H. and Glenn, Byron and Maradin, Miljenka and Pa\v{z}anin, Leo and Pogribny, Igor and Rado\v{s}, Marko and Sarnavka, Vladimir and Schulze, Andreas and Stabler, Sally and Wagner, Conrad and Zeisel, Steven H. and Mudd, Harvey}, year = {2005}, pages = {885-902}, keywords = {S-adenosylhomocysteine hydrolase deficiency, treatment}, journal = {Journal of Inherited Metabolic Disease}, volume = {28}, number = {6}, issn = {0141-8955}, title = {S-Adenosylhomocysteine hydrolase deficiency: a second patient, the younger brother of the index patient, and outcomes during therapy}, keyword = {S-adenosylhomocysteine hydrolase deficiency, treatment} }
@article{article, author = {Bari\'{c}, Ivo and \'{C}uk, Mario and Fumi\'{c}, Ksenija and Vugrek, Oliver and Allen, R.H. and Glenn, Byron and Maradin, Miljenka and Pa\v{z}anin, Leo and Pogribny, Igor and Rado\v{s}, Marko and Sarnavka, Vladimir and Schulze, Andreas and Stabler, Sally and Wagner, Conrad and Zeisel, Steven H. and Mudd, Harvey}, year = {2005}, pages = {885-902}, keywords = {S-adenosylhomocysteine hydrolase deficiency, treatment}, journal = {Journal of Inherited Metabolic Disease}, volume = {28}, number = {6}, issn = {0141-8955}, title = {S-Adenosylhomocysteine hydrolase deficiency: a second patient, the younger brother of the index patient, and outcomes during therapy.}, keyword = {S-adenosylhomocysteine hydrolase deficiency, treatment} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE





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