Publications by authors named "Mohammadreza Barzegar"

Background: Severe ankylosing spondylitis (AS) frequently involves hip joints and, occasionally, presents with concurrent spinal deformities, such as kyphoscoliosis, creating complex challenges for surgical management.

Case Presentation: We present a 26-year-old Persian male with a history of AS and severe kyphoscoliosis, leading to bilateral hip fusion and immobility. Following spinal deformity correction, a one-stage bilateral conversion to total hip arthroplasty (THA) was conducted through the direct anterior approach.

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Epidermolysis bullosa (EB) is a genotypically heterogeneous group of disorders characterized by cutaneous blistering and erosions with a tremendous spectrum of severity. One of the distinct forms of EB, Kindler EB (KEB), manifests with blistering and poikiloderma; this subtype of EB is caused by mutations in the FERMT1 gene encoding kindlin-1. In this study, we investigated a patient clinically diagnosed as KEB with reduced FERMT1 gene expression and intensity of immunostaining for kindlin-1.

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Background: Prostate specific antigen (PSA) is an important biomarker to monitor patients after treated with radiation therapy (RT). The aim of this study is to evaluate the relationship between the PSA data and prostate cancer recurrence using the joint modeling.

Methods: This historical cohort study was performed on 422 prostate cancer patients.

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Article Synopsis
  • Dystrophic epidermolysis bullosa is a genetic skin disorder that leads to severe blistering and wounds, linked to mutations in the COL7A1 gene, which encodes type VII collagen.
  • A study identified COL7A1 mutations in 152 extended Iranian families, with 104 distinct mutations found in 98% of families, reflecting a high rate of consanguinity among them.
  • Most mutations were homozygous recessive, indicating their inheritance pattern, with several previously unreported mutations and evidence of founder effects in certain cases.
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Article Synopsis
  • Autosomal recessive congenital ichthyosis is a group of disorders linked to mutations in various genes, with this study focusing on patients in Iran where consanguineous marriages are common.
  • Researchers developed a specialized gene sequencing tool targeting 38 genes related to ichthyosis and discovered six new homozygous mutations in the PNPLA1 gene among nine consanguineous families.
  • These mutations, located around the enzyme’s active center, help explain the condition's genetic diversity and can aid in genetic counseling and testing for families at risk.
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An 8-year-old boy presented with small, skin-colored papules of 9-months duration on the upper lip. Results of the histopathologic examination were consistent with syringoma. To the best of our knowledge, this is the first case report of syringoma of the mustache area of a child.

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Background: Immunofluorescence antigen mapping (IFM), is a newly introduced technique for diagnosis and classification of epidermolysis bullosa (EB) disease. The precise level of skin cleavage can be determined using monoclonal antibodies to EB-specific basement membrane zone protein.

Objective: To apply IFM technique in diagnosis and classification of EB and to identify utility and limitation of this method in our clinical setting.

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Background: The aim of this study is to evaluate the possible effects of removing the peroneus longus on the ankle and gait parameters, in order to add insufficient hamstring tendons for anterior cruciate ligament (ACL) reconstruction.

Materials And Methods: In this controlled clinical trial, 375 patients with ACL rupture who underwent ACL reconstruction arthroscopically using hamstring tendons in the orthopedic clinics of Isfahan University of Medical Sciences in 2010 and 2011 were selected. Fifteen patients were included because their hamstring tendon diameter was lower than 8 mm and peroneus longus was added.

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Old world cutaneous leishmaniasis (OWCL) usually causes a single, self-healing and uncomplicated lesion mainly on the exposed area of body. This report presents four cases of OWCL from Iran that misdiagnosed with sarcoidosis, lymphoma, and acne agminata. Two out of four patients showed a history of purplish red plaques for at least 5 years who misdiagnosed as sarcoidosis because of histological and clinical characteristics.

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