Y-type urethral duplication: an unusual variant of a rare anomaly

2004 ◽  
Vol 20 (11-12) ◽  
pp. 866-868 ◽  
Author(s):  
S. Kumaravel ◽  
R. Senthilnathan ◽  
C. Sankkarabarathi ◽  
R. K. Bagdi ◽  
S. Soundararajan ◽  
...  
Keyword(s):  
Urethral Duplication ◽  
Rare Anomaly ◽  
Unusual Variant

scholarly journals Urethral Duplication with Two Hypospadic Meati—An Unusual Variant

2016 ◽  
Vol 04 (01) ◽  
pp. 037-040 ◽  
Author(s):  
Joseph Davidson ◽  
Naomi Wright ◽  
Massimo Garriboli
Keyword(s):  
Congenital Anomaly ◽  
Male Infant ◽  
Single Stage ◽  
Type Ii ◽  
Urethral Duplication ◽  
Unique Case ◽  
Rare Congenital Anomaly ◽  
Unusual Variant ◽  
Proximal Urethra

AbstractDuplication of the urethra is a rare congenital anomaly, with approximately 300 cases reported in the literature. We report a unique case of this condition in a male infant. This case differs from the classical Effman type II-A2 duplication because of the presence of two hypospadic urethral meati, as opposed to a ventral or dorsal accessory meatus with a normally positioned distal urethra. The patient underwent a single-stage repair consisting of a proximal urethra-urethral anastomosis and distal urethral tubularization at 21 months of age with excellent results in terms of both function and cosmesis.

scholarly journals Female urethral duplication: Rare anomaly with unusual presentation

2015 ◽  
Vol 7 (1) ◽  
pp. 1 ◽  
Author(s):  
Shailesh Solanki ◽  
MNarendra Babu ◽  
Vinay Jadhav ◽  
Gowrishankar ◽  
S Ramesh
Keyword(s):  
Unusual Presentation ◽  
Urethral Duplication ◽  
Rare Anomaly

An unusual variant of urethral duplication: an addition to the Effman classification

2013 ◽  
Vol 45 (3) ◽  
pp. 601-606 ◽  
Author(s):  
Mohan K. Abraham ◽  
Saurabh Garge ◽  
Bindu Sudarshan ◽  
Naveen Vishwanath ◽  
Ramakrishnan Puzhankara ◽  
...  
Keyword(s):  
Urethral Duplication ◽  
Unusual Variant

scholarly journals Periodontal Manifestations in a Patient with Haim-Munk Syndrome

2010 ◽  
Vol 04 (03) ◽  
pp. 338-340
Author(s):  
Kamile Erciyas ◽  
Serhat Inaloz ◽  
A. Fuat Erciyas
Keyword(s):  
Autosomal Recessive ◽  
Alveolar Bone ◽  
Bone Destruction ◽  
Autosomal Recessive Disorder ◽  
Aggressive Periodontitis ◽  
Pes Planus ◽  
Rare Autosomal Recessive Disorder ◽  
Rare Anomaly ◽  
Palmoplantar Hyperkeratosis

Haim-Munk syndrome is an extremely rare autosomal recessive disorder characterized clinically by palmoplantar hyperkeratosis, aggressive periodontitis with severe alveolar bone destruction, onychogryphosis, pes planus, arachnodactyly, and acro-osteolysis. Consanguinity seems a notable prerequisite. The aim of this study was therefore to report one case of this syndrome and to focus on the periodontal manifestations, in order to attract the attention of dental clinicians to this rare anomaly. (Eur J Dent 2010;4:338-340)

scholarly journals All four coronary arteries arising separately from the right aortic sinus of Valsalva: rare anomaly

2019 ◽  
Vol 12 (4) ◽  
pp. e229498
Author(s):  
Raghvendra Choudhary ◽  
Aditya Batra ◽  
Vinay Malik ◽  
Kunal Mahajan
Keyword(s):  
Coronary Arteries ◽  
Sinus Of Valsalva ◽  
Aortic Sinus ◽  
Rare Anomaly ◽  
The Right

Bilateral absence: A rare anomaly of the gemelli muscles

Morphologie ◽  
2021 ◽  
Author(s):  
A. Abdulhameed ◽  
I.M Ahmed ◽  
S.S. Bello
Keyword(s):  
Rare Anomaly ◽  
Bilateral Absence

scholarly journals Unusual variant of invasive ductal carcinoma suggesting metaplastic melanocytic differentiation

2021 ◽  
Vol 23 ◽  
pp. 200482
Author(s):  
Chen Mayer ◽  
Maya Zilker ◽  
Nora Balint-Lahat ◽  
Rony Weitzen ◽  
Aviv Barzilai ◽  
...  
Keyword(s):  
Invasive Ductal Carcinoma ◽  
Ductal Carcinoma ◽  
Unusual Variant ◽  
Melanocytic Differentiation

scholarly journals Bilateral scrotoshisis a rare entity: case report

2021 ◽  
Vol 17 (1) ◽  
Author(s):  
Shazia Perveen ◽  
Mishraz Shaikh ◽  
Sajid Ali
Keyword(s):  
Case Report ◽  
Rare Entity ◽  
Case Presentation ◽  
Rare Anomaly ◽  
Normal Term ◽  
Twin Delivery

Abstract Background Scrotoschisis is a rare anomaly in which the testis is lying outside scrotum congenitally. Only few cases have been reported in literature under different names most of which are unilateral. We have found only one case of bilateral scrotoschisis in literature. Case presentation Newborn presented to us after normal term twin delivery as a case of bilateral scrotoschisis in which both testes were lying outside the scrotum congenitally. Baby underwent uneventful bilateral orchiopexy and was discharged home the next day. Conclusion Scrotoschisis is a very rare genital anomaly with only a few cases reported in literature. This report would add to the literature which would help in studying the exact mechanism and embryopathogenesis of this anomaly which is not known yet.

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