Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Niraj Kumar Dipak"'
Autor:
Niraj Kumar Dipak, Nadia Shagufta
Publikováno v:
Indian Pediatrics Case Reports, Vol 3, Iss 4, Pp 229-233 (2023)
Background: Infantile malignant osteopetrosis (IMO) is a rare autosomal recessive disease characterized by a higher bone density in bone marrow caused by the dysfunction of bone resorption. Clinical Description: A 2-month-old baby boy presented with
Externí odkaz:
https://doaj.org/article/a551b8bd4d814d75ba3b0a8be9e6c0ae
Publikováno v:
Journal of the Saudi Heart Association, Vol 29, Iss 3, Pp 203-210 (2017)
Ventricular outpouching is a rare finding in prenatal sonography and the main differential diagnoses are diverticulum, aneurysm, and pseudoaneurysm in addition to congenital cysts and clefts. The various modes of fetal presentation of congenital vent
Externí odkaz:
https://doaj.org/article/f585343c580848d8a6a6b0410ce1c6eb
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 18, Iss 4, Pp 330-332 (2017)
Vascular malformations (VMs) are developmental abnormalities of the vascular system. VM can be divided into high flow (predominantly arteriovenous malformations) and low flow (capillaries, venous, lymphatic, and mixed). VMs may present antenatally, a
Externí odkaz:
https://doaj.org/article/dc35aaf39d864fcaa7e45cd6af35d806
Publikováno v:
Journal of Neonatal Surgery, Vol 7, Iss 3 (2018)
Please see fulltext
Externí odkaz:
https://doaj.org/article/a6c66e1b34fb4f3c83246221a5804ade
Autor:
Niraj Kumar Dipak, Amarnath Saran
Publikováno v:
NeoReviews. 24:e326-e328
Publikováno v:
NeoReviews. 23(12)
Publikováno v:
Indian Journal of Child Health. 8:1-7
Doppler sonography provides insight into the uteroplacental and fetoplacental circulation non-invasively. It has important diagnostic implications in fetal growth restriction (FGR), monitoring of multiple pregnancies complicated by discordancy and pl
Publikováno v:
Indian Journal of Child Health. :216-219
Background: Waardenburg-Shah syndrome type 4 is an association of Waardenburg syndrome with Hirsch sprung disease. Three disease-causing genes have been identified so far: Endothelin receptor type B encoding the endothelia-B receptor, EDN3 encoding a
Publikováno v:
Journal of Paediatrics and Child Health. 57:151-152
Publikováno v:
Archives of disease in childhood - Education & practice edition. 104:160-162
A full-term (40+2/7 weeks) male baby, weighing 2.8 kg, was born to non-consanguineous parents by normal vaginal delivery. He was referred at 9 hours of age with lethargy, poor feeding, feeble cry and generalised hypotonia. On admission, he had normal