scholarly journals MURCS association and anorectal malformation: Case report of a female newborn

2017 ◽  
Vol 18 ◽  
pp. 19-23
Author(s):  
Sofia Morão ◽  
Fernando Chaves ◽  
Daniel Virella ◽  
Fátima Alves ◽  
Rui Alves ◽  
...  
2010 ◽  
Vol 4 (1) ◽  
Author(s):  
Anand Pandey ◽  
Ajay N Gangopadhyay ◽  
Vijayendra Kumar ◽  
Shiv P Sharma

2016 ◽  
Vol 29 (10) ◽  
pp. 670 ◽  
Author(s):  
Manuel Barbosa ◽  
Nuno Alves ◽  
Natacha Fontes

Perineal groove is a rare congenital anorectal malformation, with incidence yet undetermined. It is almost exclusive to the female newborn and its embryogenic origin remains uncertain. We present a case-report of a newborn girl that was discharged from the nursery without complications. At her first appointment at primary care we noted a wet sulcus connecting the posterior vaginal commissure and the anus. This case report emphasizes the rarity of the perineal groove and the importance of a good quality history and physical examination at primary care.


2010 ◽  
Vol 25 (7) ◽  
pp. 1093 ◽  
Author(s):  
Ki Hoon Ahn ◽  
Yoon Jung Boo ◽  
Hyun Joo Seol ◽  
Hyun Tae Park ◽  
Soon Cheol Hong ◽  
...  

2016 ◽  
Vol 5 (4) ◽  
pp. 274
Author(s):  
Hemanshi Shah ◽  
Charu Tiwari ◽  
Jyoti Bothra ◽  
Gursev Sandlas

2016 ◽  
Vol 5 (3) ◽  
pp. 32 ◽  
Author(s):  
Rossella Angotti ◽  
Francesco Molinaro ◽  
Anna Lavinia Bulotta ◽  
Francesco Ferrara ◽  
Marina Sica ◽  
...  

More than 50% of infants with esophageal atresia have associated anomalies. We present a case report of a 46XX neonate with long-gap esophageal atresia and tracheoesophageal fistula (EA/TEF), anorectal malformation, bowel duplication and vaginal agenesis. This is an unusual association of abnormalities which had not yet described in literature.


2006 ◽  
Vol 16 (4) ◽  
pp. 809 ◽  
Author(s):  
S Sharma ◽  
N Aggarwal ◽  
S Kumar ◽  
A Negi ◽  
JR Azad ◽  
...  

2021 ◽  
Vol 10 ◽  
pp. 33
Author(s):  
Praveen Mathur ◽  
Sharanabasappa Gubbi ◽  
Aadil Farooq ◽  
Priyanka Mittal ◽  
Gunjan Sharma

Background: Congenital pouch colon (CPC) is a rare variant of high anorectal malformation. More and more varied associations of CPC with other entities are being added to the literature. Case presentation: A 1-day-old male baby presented to the emergency room with marked abdominal distension and absent anal opening. On exploration, the baby was found to have CPC (Type 2) with colonic atresia. This association has not been reported in English literature. Conclusion: This is a report of a case of type 2 CPC with colonic atresia. To the best of our knowledge, such an association has not been reported so far. The final embryological outcome is dictated both by the topography and timing of vascular insult.


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