Zobrazeno 1 - 10
of 127
pro vyhledávání: '"Bharucha, B. A."'
Autor:
Bharucha, B.1, Padate, G. S.2 cypreabb@yahoo.com
Publikováno v:
Acta Endocrinologica (1841-0987). Jul-Sep2009, Vol. 5 Issue 3, p317-327. 11p. 2 Charts, 4 Graphs.
Publikováno v:
Journal of Postgraduate Medicine, Vol 44, Iss 4, Pp 101-4 (1998)
Prenatal diagnosis of cri-du-chat syndrome is described in 2 pregnancies. In Case 1, the mother was a balanced translocation carrier and had 2 previously affected off springs. Prenatal diagnosis by chorion villus sampling and cordocentesis was succes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::f9f8ef849450fce2e02b96940bbefcd0
http://www.jpgmonline.com/article.asp?issn=0022-3859
http://www.jpgmonline.com/article.asp?issn=0022-3859
Publikováno v:
Journal of Postgraduate Medicine, Vol 47, Iss 2, Pp 113-5 (2001)
Autosomal translocations are rare in the patients with ovarian dysgenesis. An 18-year-old female who presented with primary amenorrhoea had hypergonadotropic hypogonadism and streak ovaries with hypoplastic uterus. Karyotype analysis revealed a balan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::a641df708d2a169f627aff65e5721cb6
http://www.jpgmonline.com/article.asp?issn=0022-3859
http://www.jpgmonline.com/article.asp?issn=0022-3859
Publikováno v:
Journal of Postgraduate Medicine, Vol 46, Iss 2, Pp 98-100 (2000)
Neurofibromatosis (NF), Noonan syndrome (NS), and LEOPARD syndrome are all autosomal dominant conditions, each being a distinct clinical entity by itself. Rarely, one encounters cases with features of NF and NS and is termed as the ′Neurofibromatos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::ce45de34299fc8ad917540739190c6a1
http://www.jpgmonline.com/article.asp?issn=0022-3859
http://www.jpgmonline.com/article.asp?issn=0022-3859
Publikováno v:
Journal of Postgraduate Medicine, Vol 45, Iss 4, Pp 120-2 (1999)
A two and half year-old-male child, known case of steroid responsive nephrotic syndrome presented with fever and vomiting of acute onset. He was diagnosed to have superior sagittal sinus thrombosis on a contrast computerised tomographic scan of brain
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::1ad7105f60d65d49b680658ee90bd938
http://www.jpgmonline.com/article.asp?issn=0022-3859
http://www.jpgmonline.com/article.asp?issn=0022-3859
Publikováno v:
Journal of Postgraduate Medicine, Vol 42, Iss 3, Pp 86-8 (1996)
Three cases of cri du chat syndrome with varying ages of presentation are compared and contrasted to highlight the clinical features and evolution of the phenotype with time.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::40d928ab555cd95c50b9e786837f0a86
http://www.jpgmonline.com/article.asp?issn=0022-3859
http://www.jpgmonline.com/article.asp?issn=0022-3859
Publikováno v:
Journal of Postgraduate Medicine, Vol 39, Iss 4, Pp 228-30 (1993)
Fraser Syndrome is a rare disorder with only a few cases having been described in Indian literature. We report here a case of a patient aged 16 yr present with primary amenorrhea which is a very unusual mode of presentation. Multiple associated anoma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::af889af883a6ff9d6d4dcbfc963dc683
http://www.jpgmonline.com/article.asp?issn=0022-3859
http://www.jpgmonline.com/article.asp?issn=0022-3859
Publikováno v:
Journal of Postgraduate Medicine, Vol 38, Iss 4, Pp 180-2 (1992)
Wildervanck syndrome i.e. cervico (Klippel-Feil anomalad) -oculo (Duane-Stilling-Turk phenomenon with bilateral abducens palsy)-acoustic (deafness) is a rare syndrome. We report here 4 cases diagnosed as Wildervanck syndrome and analyse their finding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::99e2f6aeb446380a8ae158d6e7836a50
https://pubmed.ncbi.nlm.nih.gov/1307589
https://pubmed.ncbi.nlm.nih.gov/1307589
Publikováno v:
Journal of Postgraduate Medicine, Vol 45, Iss 2, Pp 58-9 (1999)
Penicillin-induced immune haemolytic anaemia is very rare. A ten year-old-female with rheumatic mitral stenosis on benzathine penicillin prophylaxis presented with features of haemolytic anaemia and investigations supported the diagnosis of immune ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::01c446bd4a411d6edfff3c7b782bd5f9
http://www.jpgmonline.com/article.asp?issn=0022-3859
http://www.jpgmonline.com/article.asp?issn=0022-3859
Autor:
Lalwani, Shivkumar, Kher, Archana, Shridhar, Nirmala, Bharucha, B., Naik, Gautami, Lalwani, S G, Kher, A, Shridhar, N, Bharucha, B A, Naik, G G
Publikováno v:
Indian Journal of Pediatrics; Sep1995, Vol. 62 Issue 5, p611-614, 4p