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Introduction: The umbilical cord anomalies directly effect on the life quality of the fetus. It can lead to fetal death or many problems during pregnancy and delivery. Early detection of these abnorma...
Netherton syndrome (NS) is a rare genodermatosis characterized by autosomal recessive inheritance pattern, unknown etiology, ichthyosiform cutaneous changes, atopic diathesis, and alterations in the h...
Background: There are accumulating evidences that Human T cell Leukemia Virus type I (HTLV-I) plays a part in the development of Sjögren's Syndrome (SS). This virus is endemic in some areas of th...
A16 year old boy was admitted to the hospital because of a swelling on the left side of mandible .He had multiple small indurated pearly papules on the head and neck with multiple well circumscribed r...
Background: This study sought to access differences in long-term (9 months) outcomes between Acute Coronary Syndrome (ACS) patients who undergo early intervention compared to Percutaneous Coronary Int...
During two years study about mitochondrial disease (Sep 1999-Agu 2001), 15 cases of Leigh syndrome (LS) were diagnosed, that consisted of 11 boys and 4 girls aged between 6 to 156 (mean: 40.5) months....
Cornelia De Lange syndrome: Report of a new case in Iran.
Down’s syndrome, or 21 trisomy, is the most common autosomal abnormality, with incidence of 1 per 815 live births in Iran. Worldwide reports indicate that about 95% are regular trisomy, or nondisjunct...
Ohtahara syndrome or ealy infantile epileptic encephalopathy is a rare cause of epileptic seizures during infancy and represents the earliest type of age related symptomatic generalized epilepsies. Th...
Finger prints of 68 patients with Down's syndrome and 93 controls have been collected and analyzed for topological of formulation of finger tip patterns suggested by Loesch (1975). The results showed ...
Background: Polycystic ovary syndrome(PCOS) is the most endocrinopathy in women and the most common causes of anovulatory infertility. Women with this disorder moreover the common manifestations such ...
Introduction: A variety of maladies, sometimes disabling, beset many ovulatory women in a recurrent manner during the luteal phase of each ovarian cycle. These problems can deteriorate interpersonal r...
We present an unknown case of an 11-year-old boy with mental retardation, microcephaly, prominent ears, unilateral ptosis, long philtrum, prominent and everted lower lip, abnormally shaped teeth and d...
Background: Reflex Sympathetic Dystrophy Syndrome (RSDS) is a rarely described complication which characterized by pain, edema, movement and vasomotor disorders, trophic changes in the skin and patchy...
Noonan syndrome is an autosomal dominant disorder that is typically evident at birth. In many affected individuals, this syn­drome is associated with cardiac defects and a distinctive facial appea...

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