Author/Authors :
MOHAMMADI PARGOO، Esmaeel نويسنده Science and Research Branch of Islamic , , ARYANI، Omid نويسنده Senior Researcher, Molecular Genetics, Department of Medical Genetics, Special Medical Center, Tehran, Iran , , TONEKABONI، Seyyed Hassan نويسنده Associate Professor of Pediatric Neurology, Pediatric Neurology Research Center, Department of Pediatric Neurology, Shahid Beheshti University of Medi , , Yaghmaei، Parichehr نويسنده Islamic Azad University, Science and Research Branch, Tehran, Iran , , Houshmand، Massoud نويسنده ,
Abstract :
Abstract
As a result of higher distributed consanguinity in the Mediterranean region and
the Middle East, autosomal-recessive forms of Charcot-Marie-Tooth (ARCMT)
are more common in these areas. CMT disease caused by mutations in the
ganglioside-induced differentiation-associated protein 1 (GDAP1) gene is a
severe autosomal recessive neuropathy resulting in either demyelinating CMT4A
neuropathy or axonal neuropathy with vocal cord paresis. The patient was an
8-year-old boy with AR inheritance that showed some delayed achievement of
motor milestones, including walking, also bilateral foot drop, wasting of distal
muscles in the legs, pes cavus and marked weakness of the foot dorsiflexors. He
had no hoarseness or vocal cord paralysis. Total genomic DNA was extracted
from whole peripheral blood of the patient and his family by using standard
procedures. PCR- sequencing method were used to analysis the whole coding
regions of the GDAP1 gene. A novel homozygote insertion of T nucleotide
in codon 34 was detected (c.100_101insT) that probably led to an early stop
codon. This mutation may be associated with a common haplotype, suggesting
a common ancestor that needs further investigation in the Iranian population.