Zobrazeno 1 - 10
of 26
pro vyhledávání: '"V Shankar Raman"'
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 27, Iss 6, Pp 764-767 (2022)
Pediatric adrenocortical tumors (ACTs) are rare entities with an incidence of 0.2% of all pediatric tumors. Only two cases of antenatally detected ACT have been reported in the literature. Our case is the first report of an antenatally detected supra
Externí odkaz:
https://doaj.org/article/a8d4db6952f841e2aab1cabe4250ebf3
Publikováno v:
African Journal of Paediatric Surgery, Vol 19, Iss 4, Pp 233-237 (2022)
Background and Objectives: Undescended testes (UDT) or cryptorchidism is a common congenital disability characterised by the absence of at least one testicle from the scrotum. The primary aim of surgical correction is to preserve fertility potential
Externí odkaz:
https://doaj.org/article/290b612e3825462b9273b15eb553a650
Autor:
V Shankar Raman, Sandeep Agarwala, Veereshwar Bhatnagar, Shasanka Shekhar Panda, Arun Kumar Gupta
Publikováno v:
Lung India, Vol 32, Iss 2, Pp 116-118 (2015)
Background: A majority of cystic lesions in the western world are detected antenatally, whereas, the diagnosis in our setup occurs once the child becomes symptomatic. Surgical management is primarily dictated by the presence of symptoms, recurrent in
Externí odkaz:
https://doaj.org/article/71df9d5dd95943b4ae21dd0b6a41a8d5
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 19, Iss 4, Pp 246-246 (2014)
Externí odkaz:
https://doaj.org/article/f92d1210f83a47bcaedab07bc3f7a6cf
Publikováno v:
Medical Journal Armed Forces India.
Publikováno v:
Fetal and pediatric pathology.
Hypospadias is a common congenital abnormality typified by a proximally placed ectopic urethral meatus along the ventral surface of the penis. Androgen receptor (AR) and estrogen receptor (ER) expression in the hypospadias tissues may be altered in h
Publikováno v:
Med J Armed Forces India
Background Cloacal anomalies are the severest and most complex of all anorectal malformations (ARMs). They require careful evaluation and meticulous surgery tailored to suit each variant. We present our experience in a series of nine cases. Methods T
Publikováno v:
Med J Armed Forces India
An 11-year-old female patient presented with congenital spinal deformity with a history of occasional pain in the right flank for a duration of six months. On evaluation, she was diagnosed to be a case of type III Klippel Feil syndrome (KFS) with cro
Publikováno v:
Medical Journal Armed Forces India.
Publikováno v:
Journal of Pediatric Surgery. 53:2112-2116
Background Congenital pyloric atresia (CPA) is a rare anomaly with an incidence of 1 in 100,000 live births. Depending on the type of anomaly patients can either present in the neonatal period or later in life with subtle nonspecific signs and sympto