El-Hattab AW, Scaglia F. Mitochondrial DNA depletion
syndromes: review and updates of genetic basis, manifestations, and therapeutic
options. Neurotherapeutics. 2013 Apr;10(2):186-98.
Abstract
Mitochondrial DNA (mtDNA) depletion syndromes (MDS) are a
genetically and clinically heterogeneous group of autosomal recessive disorders
that are characterized by a severe reduction in mtDNA content leading to
impaired energy production in affected tissues and organs. MDS are due to
defects in mtDNA maintenance caused by mutations in nuclear genes that function
in either mitochondrial nucleotide synthesis (TK2, SUCLA2, SUCLG1, RRM2B,
DGUOK, and TYMP) or mtDNA replication (POLG and C10orf2). MDS are
phenotypically heterogeneous and usually classified as myopathic, encephalomyopathic,
hepatocerebral or neurogastrointestinal. Myopathic MDS, caused by mutations in
TK2, usually present before the age of 2 years with hypotonia and muscle
weakness. Encephalomyopathic MDS, caused by mutations in SUCLA2, SUCLG1, or
RRM2B, typically present during infancy with hypotonia and pronounced
neurological features. Hepatocerebral MDS, caused by mutations in DGUOK, MPV17,
POLG, or C10orf2, commonly have an early-onset liver dysfunction and
neurological involvement. Finally, TYMP mutations have been associated with
mitochondrial neurogastrointestinal encephalopathy (MNGIE) disease that
typically presents before the age of 20 years with progressive gastrointestinal
dysmotility and peripheral neuropathy. Overall, MDS are severe disorders with
poor prognosis in the majority of affected individuals. No efficacious therapy
is available for any of these disorders. Affected individuals should have a
comprehensive evaluation to assess the degree of involvement of different
systems. Treatment is directed mainly toward providing symptomatic management.
Nutritional modulation and cofactor supplementation may be beneficial. Liver
transplantation remains controversial. Finally, stem cell transplantation in
MNGIE disease shows promising results.
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