Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary disorder (estimated prevalence of 1 per 1000–1 2500 live births)1 characterized by development and growth multiple bilateral cysts eventually leading to end-stage renal replacement therapy.1

Recently multiple cutaneous leiomyomas, uterine leiomyoimatosis and renal cancer have been described as a cancer syndrome with autosomal dominant pattern of inheritance.We report a 79-year-old man who presented with multiple hyperkertotic erythematous nodules on his right leg with histological diagnosis of pilar leiomyoma. In his past medical history several systemic co...

-Objective. Goldenhar syndrome (oculoauriculovertebral dysplasia) is associated with anomalies in multiple organ systems. Renal abnormalities have also been reported with the complex, but the incidence of associated genitourinary malformations has not been defined. Method. We have reviewed our experience with 28 children with Goldenhar syndrome evaluated during the past twelve years. Twenty chi...

Muller cyst is very rare. It found in about 5% of azoosperm patients. a residual embryological vestige the female genital organ men. collection developed uterine cavity man called prostatic utricle. [1] it benign lesion, most often congenital, rarely acquired. This lesion may be asymptomatic or symptomatic, and rare cases associated with renal agenesis. [2] various means treatment, treatment co...

CASE REPORT The patient was a 26 year old man who presented with typical symptoms of endstage renal failure in December, 1971. Prior to this he had always been well, though his mother remembered that he had a "chill on the kidneys" at the age of 6 years. The family history was negative for renal disease. He had a twin brother. On examination he was clinically anaemic and uraemric. Blood pressur...