A Congenital Abnormality of the Uterus and Vagina

نویسنده

  • G. B. Archer
چکیده

A Mohammedan woman, aged 19, complained of abdominal pain of a very distressingcharacter. A tumour was present in the lower abdomen gradually increasing in size; and no menstruation. The woman had been deserted by her husband. Examination showed a movable tumour in the position and size of a fiva month's pregnancy. The vagina was shallow, about li inches in depth, and a blind sac. The cervical end of the uterus could be felt separated by

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Congenital absence of the uterus and vagina is not commonly transmitted as a dominant genetic trait: outcomes of surrogate pregnancies.

OBJECTIVE To determine the inheritance pattern of congenital absence of the uterus and vagina in affected women undergoing surrogacy IVF with this disorder. DESIGN Retrospective study. SETTING A hospital-based reproductive endocrinology and infertility center. PATIENT(S) Women diagnosed with congenital absence of the uterus and vagina undergoing IVF with subsequent transfer of embryos to ...

متن کامل

Association of unilateral renal agenesis and genital anomalies

Congenital unilateral renal agenesis occurs in 0.93–1.8 per 1000 autopsies, and is usually diagnosed on an incidental imaging examination. Genital anomalies occur in 37–60% of females and 12% of males with congenital unilateral renal agenesis. Abnormalities in females include agenesis, duplication, rudimentary, unicornuate or bicornuate uterus, double or absent vagina, absent or hypoplastic ova...

متن کامل

Mayer-Rokitansky-Kuster-Hauser Syndrome.

Mayer-Rokitansky-Küster-Hauser Syndrome is a congenital malformation in which there is failure of the Müllerian ducts to develop resulting in absent uterus and fallopian tubes and variable malformations of the vagina. Ultrasonography reveals absence of uterus with normally visualised ovaries.

متن کامل

Uterine Malformations

In the female, Müllerian ducts will develop to form the uterine tubes, uterus, cervix, and the upper one-third of the vagina; in the male, they are lost. This abnormal development can lead to uterine malformations resulting from aplasia of a part of Müllerian duct. Morphological abnormalities can vary from insufficient fission of tissues causing bicornuate uterus, double uterus or preserved ute...

متن کامل

Uterine Malformations

In the female, Müllerian ducts will develop to form the uterine tubes, uterus, cervix, and the upper one-third of the vagina; in the male, they are lost. This abnormal development can lead to uterine malformations resulting from aplasia of a part of Müllerian duct. Morphological abnormalities can vary from insufficient fission of tissues causing bicornuate uterus, double uterus or preserved ute...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره 59  شماره 

صفحات  -

تاریخ انتشار 2016