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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...
Lip pits are among the rarest congenital deformities recorded. Initially reported in 1845, it’s familial occurrence has been reported just once. These developmental anomalies occur either as an isolat...
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...
PagetÕs disease of the breast is a rare condition with an incidence of 1-4.3% of all mammary malignancies. Of all malignant breast cancers, 1% occur in male patients, and thus PagetÕs di...
Background: Lethal toxic encephalopathy of shigellosis (Ekiri syndrome) is a rare complication of the shigella infection presented with fever, severe toxicity, seizure and diffuse brain edema, coma an...
The incidence of anomalies is high in multiple gestations especially in monochorionic twins. This paper reported a case of an acardiac parabiotic twin, a rare deformed fetus which occurs typically in ...
Objective: Congenital chloride diarrhea (CCD) is a rare autosomal recessive disorder of intestinal chloride absorption. Pathognomonic features consist of watery diarrhea, failure to thrive, dehydratio...
Objective: To report the case of a 46-year old male with major depressive disorder, who represented manic symptoms, when olanzapine was added to his treatment. Method: A 46-year old female, with a dia...
Moebius Syndrome is a rare congenital disorder of the facial and abducens nerve. Other cranial nerves may be involved, such as V, IX and XII. Several central nervous system anomalies including hypopla...

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