Ranging from aplastic uterus (including Mayer–Rokitansky–Kuster–Hauser syndrome) to
incomplete septate uterus, uterine malformations as a group are relatively frequent in the …

Woodhouse‐Sakati syndrome (WSS) is a rare autosomal recessive neuroendocrine and
ectodermal disorder caused by variants in the DCAF17 gene. In Qatar, the c. 436delC …

Objective The dual diagnosis of hypoplastic uterus in association with ovarian dysgenesis is
regularly reported but the pathogenesis of the association is unclear. The uterus, however …

Gonadal dysgenesis and Mayer-Rokitansky-Küster-Hauser syndrome (MRKHS) are the
most common causes of primary amenorrhoea. Patients with gonadal dysgenesis present …

The association of gonadal dysgenesis and Mayer-Rokitansky-Kuster-Hauser syndrome is
very rare. We report a 21-year-old phenotypical female who presented with primary …

Background Turner syndrome is a common chromosomal disorder, with an incidence of 1 in
2000 live-born female infants. Mayer-Rokitansky-Küster-Hauser syndrome (MRKH) affects 1 …

There is perhaps no region with a richer history or a more diverse ethnic, cultural and
religious makeup than the Arab world. It is the cradle of civilization and birthplace of the …

Turner syndrome is a relatively common chromosomal abnormality presenting as primary
amenorrhoea in gynaecological and endocrine clinics, caused by complete or partial X …

Introduction: Phenotypically normal pre-pubertal girl presenting with only a little delay in
onset of puberty and emotional lability is seldom thought to be suffering from a serious …

Introduction: Le syndrome de Mayer-Rokitanski-Küster-Hauser (MRKH) reste une cause
rare de l´ aménorrhée primaire. Le but de cette étude était d'évaluer la place de l'examen …