Zobrazeno 1 - 10
of 65
pro vyhledávání: '"M. Narendra Babu"'
Autor:
Jayalaxmi Shripati Aihole, Aruna Gowdra, Deepak Javaregowda, Vinay Jadhav, M Narendra Babu, Ravidra Sahadev
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 23, Iss 3, Pp 131-139 (2018)
Background: Congenital diaphragmatic hernia (CDH) is a complex developmental defect having a multifactorial etiology; i majority of cases (~80%), the cause is not known. Survival rates for patients with CDH have increased over the past decade with ea
Externí odkaz:
https://doaj.org/article/679c1297fad842a9af494c202a1e1856
Publikováno v:
African Journal of Urology, Vol 22, Iss 3, Pp 196-198 (2016)
Introduction: Congenital prepubic sinus (CPS) is a rare anomaly. It has been considered as one of the presentations of the spectrum of vesico urethral developmental defects. Observations: We are reporting two such rare cases: one in a year old female
Externí odkaz:
https://doaj.org/article/69a58ea6cfbb449d938890b3fa3eada5
Publikováno v:
Indian Journal of Plastic Surgery, Vol 49, Iss 01, Pp 106-108 (2016)
A new-born male presented within 12 h of birth with respiratory distress. On examination and workup, he had palatoglossal fusion, cleft palate and hypoplasia of the cerebellar vermis. A 2.5 Fr endotracheal tube was inserted into the pharynx through n
Externí odkaz:
https://doaj.org/article/0263169162104c6698bfa4b76db1f9e1
Publikováno v:
Urology Annals, Vol 7, Iss 1, Pp 104-106 (2015)
Persistent Mullerian duct syndrome (PMDS) is a rare form of Disorder of sex development in which Mullerian duct derivatives (fallopian tubes, uterus and the proximal vagina) are present in an otherwise normally differentiated 46 XY male. In the major
Externí odkaz:
https://doaj.org/article/5432e30e22be43c8a3cc925bbe696111
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 20, Iss 1, Pp 45-47 (2015)
Rectal duplication (RD) accounts for 5% of alimentary tract duplication. A varied presentation and associated anomalies have been described in the literature. Antenatal rupture of the RD is very rare. We present an unusual case of a ruptured RD assoc
Externí odkaz:
https://doaj.org/article/831115a7d6734e72a4af940e0670ecc1
Autor:
Harish Prabhudev, M. Narendra Babu, Pavuluri Aravind Kumar, Deepika Gorantla, Kalapala Raviraj, S.V.V.S. Musalaiah
Publikováno v:
International Journal of Advanced Research. 8:501-507
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 22, Iss 3, Pp 163-164 (2017)
Clitoral hypertrophy is usually seen as a congenital malformation, specifically during the stages of hormonal expressions in the disorders of sexual development. Acquired clitoral hypertrophy is a relatively rare condition. Clitoris can be the site o
Externí odkaz:
https://doaj.org/article/6b95d36f3b5c411e88ca47b02f64bce3
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 18, Iss 4, Pp 162-164 (2013)
We present a rare case of mediastinal hemangioma in a 4-year-old child. The child presented with cough and fever and the chest radiograph revealed right pleural effusion. On further work-up with chest computed tomography mediastinal cystic mass occup
Externí odkaz:
https://doaj.org/article/f31d5a85f2c2444897a360cc1530877c
Publikováno v:
Journal of Biomedical and Pharmaceutical Research. 9
Treatment of gingival recession has become an important therapeutic issue due to increasing cosmetic demand. Multiple surgical procedures have been developed to obtain predictable esthetic root coverage.. Low level laser therapy (LLLT) has biostimula
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 17, Iss 3, Pp 124-125 (2012)
Extrarenal calyces are one of the rare renal anomalies associated with the collecting system. Their association with renal ectopia or horse shoe kidney is known. But, here in, we are reporting an intraoperative surprise, where extrarenal calyces were
Externí odkaz:
https://doaj.org/article/a18cef6b066e4e22909b9455315bc7bf