Mayer-Rokitansky Kuster Hauser (MRKH) syndrome with lieomyoma is a rare disorder. Women this have normal 46 XX karyotype, secondary sex characteristics and primary amenorrhea. There scarcity of cases in the literature where fibroid develops women suffering from MRKH syndrome. Here, we present case an ectopic broad ligament found 41-year-old woman type II. A married nulliparous female diagnosed ...

Inheritance Bazex-Dupré-Christol syndrome is an X-linked dominant genodermatosis, with a prevalence below 1/1 000 000. The female to male ratio reaches the expected 2:1, and females appear to be less affected than males. There is intrafamilial and interfamilial phenotypic variability (Lacombe and Taïeb, 1995; Kidd et al., 1996). Most cases are European patients. Oley syndrome (Oley et al., 1992...

Previous studies have demonstrated that the metabolic syndrome is associated with impaired skeletal muscle arteriolar function, although integrating observations into a conceptual framework for impaired perfusion in peripheral vascular disease (PVD) has been limited. This study builds on previous work to evaluate in situ arteriolar hemodynamics in cremaster muscle of obese Zucker rats (OZR) to ...

Adrenal cortical tumors constitute a heterogeneous group of neoplasms with distinct clinical, morphological, and molecular features. Recent discoveries of specific genotype-phenotype correlations in adrenal cortical adenomas have transformed our understanding of their respective endocrine syndromes. Indeed, a proportion of patients with primary aldosteronism are now known to harbor adrenal cort...

Membranoproliferative glomerulonephritis describes a glomerular-injury pattern common to heterogeneous group of diseases. Evaluation based on clinical and laboratory presentation immunofluorescence staining kidney biopsy allows identification underlying pathophysiological processes may facilitate proper diagnosis treatment. Hypocomplementemic urticarial vasculitis syndrome is rare autoimmune di...