Results 121 to 130 of about 1,327,945 (260)

Fetal MRI : an essential step in interpreting complex ultrasound findings [PDF]

, 2016
Background: Fetal magnetic resonance imaging (MRI) allows for the interpretation of complex fetal anomalies detected on ultrasound (US). Locally it has been available since 2013 but has remained underused.
Baldacchino, Ian, Gatt, Andre Stefan, Saliba, Isabelle   +2 more
core  

Fraser of cryptophthalmosis syndrome: A case report [PDF]

, 2004
Fraser or cryptophthalmos syndrome is a rare autosomal recessive disorder characterized by major features such as cryptophthalmos, syndactyly, and abnormal genitalia. Consanguinity is reported in 15-24.8% of the cases.
Adibi, B., Golalipour, M.-J., Haidary, K., Khoury, E.   +3 more
core  

Robert's uterus with ipsilateral renal agenesis presenting as pelvic inflammatory disease in a teenager: A case report

Journal of Pediatric Surgery Case Reports
Introduction: Robert's uterus, with ipsilateral renal agenesis, is an exceptionally rare Mullerian duct anomaly (MDA). It usually presents with cyclical pain, but presentation as pelvic inflammatory disease in an adolescent is extremely uncommon.
Akkamahadevi C. Hiremath, Harshita Ramamurthy, T.D. Nandeesha, R. Padmasri   +3 more
doaj   +1 more source

Central blood volume in cirrhosis [PDF]

, 1993
Bendtsen, Flemming, Gerbes, Alexander L., Henriksen, Jens H.   +2 more
core   +1 more source

Zinner syndrome: Late-Diagnosis in a 55-year-old male and favorable outcome after surgical excision - A case report and review of the literatureKey points

Urology Case Reports
Zinner Syndrome (ZS) is a rare congenital anomaly defined by the triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ejaculatory duct obstruction. We report a 55-year-old male presenting with chronic perineal pain and LUTS.
Kinh Luan Thai, Duy Dien Nguyen, Do La Quach, Nho Tinh Le, Le Quy Van Dinh, Minh Dinh Nguyen, Ryan Dobbs, Ho Trong Tan Truong, Tuan Thanh Nguyen, Xuan Thai Ngo   +9 more
doaj   +1 more source

Diagnosis of femoral hypoplasia-unusual facies syndrome in the fetus. [PDF]

, 2007
D'ARMIENTO, MARIA, Leone F, MARTINELLI, PASQUALE, Maruotti GM, PALADINI, DARIO, Penner I, Sglavo G   +6 more
core   +1 more source

A case of congenital unilateral absence of the vas deferens

International Medical Case Reports Journal, 2013
Bi Mo,1 Vishnu Garla,2 Lawrence M Wyner1 1Department of Surgery, 2Department of Internal Medicine, Marshall University, Huntington, WV, USA Background: Congenital unilateral absence of the vas deferens occurs in 0.5%–1.0% of males.
Mo B, Garla V, Wyner LM
doaj  

NEFROPATÍA POR ENFERMEDAD DE FABRY ASOCIADA A AGENESIA RENAL CONGÉNITA

Revistas Argentina de Medicina, 2017
Se presenta una mujer de 42 años de edad con agenesia renal congénita y enfermedad de Fabry, una asociación no comunicada hasta la fecha. Ambas patologías son posibles causas de proteinuria. Por la contraindicación relativa que significa la presencia de
Sebastián Pedro Antonio Jaurretche
doaj  

False-positive PSMA uptake from urinary reflux into a seminal vesicle cyst in renal agenesis. [PDF]

Radiol Case Rep
Ting CH, Singh D, Yaxley J.
europepmc   +1 more source

Obstructed Hemi-Vagina with Ipsilateral Renal Agenesis Syndrome in Adulthood: A Diagnostic Challenge. [PDF]

Diagnostics (Basel), 2023
Grammatis AL, Ajibade F, Warakaulle D, Dada T.   +3 more
europepmc   +1 more source