scholarly journals Diphallia with Associated Anomalies: A Case Report and Literature Review

2013 ◽  
Vol 2013 ◽  
pp. 1-4 ◽  
Author(s):  
Pande Made Wisnu Tirtayasa ◽  
Robertus Bebet Prasetyo ◽  
Arry Rodjani
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Literature Review ◽  
Pubic Symphysis ◽  
Associated Anomalies ◽  
Rare Congenital Anomaly ◽  
Live Births ◽  
Pubic Symphysis Diastasis ◽  
Symphysis Diastasis

Diphallia or penile duplication is an extremely rare congenital anomaly. It occurs once in every 5.5 million live births. The extent of penile duplication and the number of associated anomalies vary greatly, ranging from a double glans from a penis with no associated anomaly up to complete penile duplication associated with multiple anomalies. Here, we report a 12-year-old boy with complete bifid diphallia associated with bifid scrotum, epispadia, and pubic symphysis diastasis along with a review of the articles pertaining to this anomaly.

scholarly journals Pubic Symphysis Diastasis: A Case Series and Literature Review

2017 ◽  
Vol 32 (6) ◽  
pp. 510-514 ◽  
Author(s):  
Jaya Jethra Chawla ◽  
Devendra Arora ◽  
Namrita Sandhu ◽  
Megha Jain ◽  
Anju Kumari
Keyword(s):  
Literature Review ◽  
Case Series ◽  
Pubic Symphysis ◽  
Pubic Symphysis Diastasis ◽  
Symphysis Diastasis

scholarly journals Severe Pubic Symphysis Diastasis Managed Conservatively: A Case Report and Review

2017 ◽  
Vol 06 (04) ◽  
pp. 120-126 ◽  
Author(s):  
Vijay Palvia ◽  
Susan Kim ◽  
Holli Warholic ◽  
James Anasti
Keyword(s):  
Case Report ◽  
Pubic Symphysis ◽  
Pubic Symphysis Diastasis ◽  
Symphysis Diastasis

Pubic symphysis diastasis after an uncomplicated vaginal delivery: A case report

2014 ◽  
Vol 35 (7) ◽  
pp. 746-747 ◽  
Author(s):  
F. Saeed ◽  
K. Trathen ◽  
A. Want ◽  
R. Kucheria ◽  
S. Kalla
Keyword(s):  
Case Report ◽  
Vaginal Delivery ◽  
Pubic Symphysis ◽  
Pubic Symphysis Diastasis ◽  
Symphysis Diastasis

BILATERAL BIPARTITE CARPAL SCAPHOID: A CASE REPORT AND LITERATURE REVIEW

Hand Surgery ◽  
2014 ◽  
Vol 19 (03) ◽  
pp. 427-431
Author(s):  
Yoshiharu Takemitsu ◽  
Yoshikazu Nakayama ◽  
Hideki Ota ◽  
Yoshiyuki Matsumoto ◽  
Hirotaka Kida
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Literature Review ◽  
Degenerative Change ◽  
Rare Congenital Anomaly ◽  
History Of ◽  
Diagnostic Differentiation

Congenital bipartite carpal scaphoid has been reported as an extremely rare congenital anomaly. We report a case of a 47-year-old man who was found with bilateral bipartite carpal scaphoids with no history of injury. Radiographs demonstrated symmetric findings of the distinct bipartition of the scaphoid without obvious degenerative change in both wrists. The patient complained of no other symptoms. The diagnostic differentiation of scaphoid bipartition from the pseudarthrosis of the scaphoid could be important in avoiding unnecessary surgery and inappropriate assessment in compensation cases.

CONGENITAL METACARPAL SYNOSTOSIS TREATED BY DOUBLE BONE BLOCKS TECHNIQUE: A CASE REPORT FROM THAILAND

Hand Surgery ◽  
2005 ◽  
Vol 10 (01) ◽  
pp. 131-134 ◽  
Author(s):  
Surut Jianmongkol ◽  
Tala Thammaroj ◽  
Kitiwan Vipulakorn
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Surgical Techniques ◽  
Rare Condition ◽  
Rare Congenital Anomaly

Congenital metacarpal synostosis is a rare congenital anomaly in the hand, especially in our area. There were several reports of surgical techniques for correction deformities. We report this rare condition in our hospital and treatment with the metacarpal osteotomy and double bone blocks technique of grafting.

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