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

Abstract

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 aetiology. The latter include, most importantly, markedly elevated plasma AdoHcy. Plasma S-adenosylmethionine (AdoMet) is also elevated, as is methionine (although the hypermethioninaemia may be absent or nonsignificant 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.

• Authors: I Barić, M Cuk, K Fumić, O Vugrek, R H Allen, B Glenn, M Maradin, L Pazanin, I Pogribny, M Rados, V Sarnavka, A Schulze, S Stabler, C Wagner, S H Zeisel, S H Mudd
• Journal: Journal of inherited metabolic disease (J Inherit Metab Dis) Vol. 28 Issue 6 Pg. 885-902 ( 2005) ISSN: 0141-8955 [Print] United States
• PMID: 16435181 (Publication Type: Case Reports, Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.)

Chemical References

• Amino Acids
• Methionine
• Transaminases
• Creatine Kinase
• Adenosylhomocysteinase

Topics

• Adenosylhomocysteinase (deficiency, genetics)
• Amino Acids (chemistry)
• Brain (pathology)
• Child, Preschool
• Creatine Kinase (blood)
• Croatia
• DNA Methylation
• Erythrocytes (metabolism)
• Exons
• Family Health
• Humans
• Infant
• Magnetic Resonance Imaging
• Magnetic Resonance Spectroscopy
• Male
• Methionine (metabolism)
• Mutation
• Myelin Sheath (chemistry)
• Time Factors
• Transaminases (blood)
• Treatment Outcome