MURCS association (a variant of Mayer-Rokitansky-Küster-Hauser syndrome) is a very rare developmental disorder [2] that primarily affects the reproductive and urinary systems involving MUllerian agenesis, Renal agenesis, Cervicothoracic …

MURCS (Müllerian duct aplasia–renal agenesis–cervicothoracic somite dysplasia) association is a rare developmental disorder with four common malformations specifically described as uterine hypoplasia or aplasia, renal agenesis or ectopy, vertebral anomalies and …

Müllerian duct aplasia-renal aplasia-cervicothoracic somite dysplasia (MURCS) association is a unique development disorder with four common types of malformations that include uterine aplasia or hypoplasia, renal ectopy or agenesis, vertebral ...

MURCS is an acronym that stands for MÜllerian duct aplasia, Renal aplasia, Cervicothoracic Somite dysplasia. It is a very rare disorder that affects only females.

2014年7月4日 · Learn about Mayer-Rokitansky-Küster-Hauser Syndrome, including symptoms, causes, and treatments. If you or a loved one is affected by this condition, visit Patients & Caregivers

2021年4月4日 · Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome type 2, a form of MRKH syndrome (see this term), is characterized by congenital aplasia of the uterus and upper 2/3 of the vagina that is associated with at least one other malformation such as renal, vertebral, or, less commonly, auditory and cardiac defects.

2024年1月20日 · MURCS syndrome stands for mullerian duct aplasia, renal anomalies, and cervicothoracic somite anomalies. This is an atypical manifestation of MRKH (Mayer–Rokitansky–Kuster–Hauser) syndrome and is classified as MRKH type 2.

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome type 2, a form of MRKH syndrome (see this term), is characterized by congenital aplasia of the uterus and upper 2/3 of the vagina that is associated with at least one other malformation such as renal, vertebral, or, less commonly, auditory and cardiac defects.

What is Mayer-Rokitansky-Küster-Hauser Syndrome? Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome, also known as Müllerian agenesis or vaginal agenesis, is a rare congenital condition affecting the development of female reproductive organs.

MURCS association, which stands for Müllerian duct aplasia (MU), congenital renal dysplasia (R), cervical somite anomalies (CS), is the atypical (or type II) form of Mayer-Rokitansky-Küster-Hauser syndrome, characterised by utero-vaginal atresia in otherwise normal females as well associated kidney and skeletal abnormalities and hearing problems.