Nunes, Natalie and Karandikar, Sharad S and Cooper, Sarah and Jaganathan, Ramasamy and Irani, Shirin (2009) VATER/VACTERL syndrome (vertebra/anus/cardiac/trachea/esophogus/radius/renal/limb anomalies) with a noncommunicating functioning uterine horn and a unicornuate uterus: a case report. Fertility and sterility, 91 (5). 1957.e11-2. ISSN 1556-5653. This article is accessible to all HEFT staff and students via NHS Evidence www.evidence.nhs.uk by using their HEFT Athens login IDsFull text not available from this repository. (Request a copy)
To describe the presentation and outcome of a patient with an unusual association of VATER/VACTERL syndrome (vertebra/anus/cardiac/trachea/esophogus/radius/renal/limb) and noncommunicating functioning uterine horn and a unicornuate uterus.
Descriptive case report.
A foundation trust in the United Kingdom. MATERIALS AND METHOD(S): A patient known to have VATER/VACTERL syndrome was diagnosed with a hematometra of a noncommunicating uterine horn and hematosalpinx. She underwent multidisciplinary surgery to remove the functioning uterine horn, after which she had a full recovery.
This case documents the association of VATER/VACTERL syndrome with a unicornuate uterus and noncommunicating horn.
|Additional Information:||This article is accessible to all HEFT staff and students via NHS Evidence www.evidence.nhs.uk by using their HEFT Athens login IDs|
WQ Obstetrics. Midwifery
|Divisions:||Planned IP Care > General Surgery
Planned IP Care > Urology
Womens and Childrens > Gynaecology
|Depositing User:||Sophie Rollason|
|Date Deposited:||10 Jun 2014 13:32|
|Last Modified:||10 Jun 2014 13:32|
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