Sanjad-Sakati Syndrome, also referred to as Hypoparathyroidism-Retardation-Dysmorphism Syndrome or Middle East was first reported in Saudi Arabia 1988 and later a definitive report by (Sanjad et al.) 1991. It is rare autosomal recessive condition almost exclusively the Arab population. The characterized an extensive array of symptoms, including congenital hypoparathyroidism, severe growth devel...

Several chronic liver diseases are characterized by a clear gender disparity. Among them, hepatocellular carcinoma (HCC) shows significantly higher incidence rates in men than women. The different epidemiological distribution of risk factors for disease and HCC only partially accounts these differences. In fact, the is an organ with recognized sexual dysmorphism extremely sensitive to action an...

schwartz-jampel syndrome, (sjs) is a rare disorder characterized by myotonia, joint contracture, facial dysmorphism and growth retardation, we present three siblings (two sisters and one brother) 19,24 and 27 years old from consanguineous healthy parents with sjs. their clinical features were similar to those previously described. motor and sensory nerve conduction study (ncs) were compatible w...

small-sized hyaline casts, Ͻ4 in each slide; hyaline with medium or large diameter, cellular, granular, granulo-hematic, waxy casts, none; cystine crystals, none; other crystals, rare (Ͻ10 in each slide). We usually notice a high prevalence of pathologic findings (ϳ70%) in microscopic analysis of urine samples from our patients. Applying the published algorithm, we estimated that only 93 sample...

study question: Is it time to reconsider whether oocytes affected by smooth endoplasmic reticulum aggregates (SERa) should still be destroyed? summary answer: At the time of writing, the literature shows that 171 apparently healthy babies have been born from SERa+ cycles amongst which 22 were from SERa+ oocytes. what is known already: The SER dysmorphism has been associated with negative embryo...