Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Sachin, Daigavane"'
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 18, Iss 04, Pp 01-03 (2024)
Marfan syndrome is an autosomal dominant hereditary connective tissue disease caused by mutations in the Fibrillin-1 gene located on chromosome 15q15-21. Fibrillin is a specific type of glycoprotein widely distributed throughout the body, contributin
Externí odkaz:
https://doaj.org/article/06845e5527e146b3ae5e1c50d4243ae2
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 18, Iss 03, Pp 01-03 (2024)
Aniridia is characterised by variable degrees of hypoplastic iris or complete absence of iris tissue and is a rare congenital disorder. Mutation in the PAX6 gene is mostly responsible for aniridia. It is associated with various ocular manifestations
Externí odkaz:
https://doaj.org/article/31eb5441c1ac4d89a48fa214a05bcea1
Autor:
Raina Jain, Sachin Daigavane
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 18, Iss 06, Pp 01-02 (2024)
A fatal viral infection called rubella, often known as German or three-day measles, is spread by the Rubivirus genus of the Togaviridae family. The disorder known as Congenital Rubella Syndrome (CRS) has the potential to cause a wide range of multisy
Externí odkaz:
https://doaj.org/article/c35f86d639024d1fae3e93c5ddd3ce14
Autor:
Rasika Bagewadi, Sachin Daigavane
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 17, Iss 1, Pp NJ01-NJ02 (2023)
The manuscript presents a 43-year-old male farmer who came to the Ophthalmology Outpatient Department (OPD) for his routine ophthalmological examination. No significant family history was elucidated. On clinical examination, his unaided Visual Acuity
Externí odkaz:
https://doaj.org/article/412c6e8b11bd44ad9809f34ba9511d79
Autor:
Kervi N Mehta, Sachin Daigavane
Publikováno v:
Indian Journal of Ophthalmology, Vol 70, Iss 7, Pp 2684-2686 (2022)
Externí odkaz:
https://doaj.org/article/b1d0d91c7ca044798641f7f73e29dc0f
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 16, Iss 8, Pp OD04-OD06 (2022)
Non arteritis Anterior Ischaemic Optic Neuropathy (NAION) is mentioned as loss of blood supply to the optic nerve further causing sudden onset and painless vision loss in eye. Exact mechanism, leading to reduced or loss of flow of blood to an optic n
Externí odkaz:
https://doaj.org/article/a6ae136bb62b4a77af4b91579892fd5e
Publikováno v:
Medical Science. 27:1-6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::169bd58ae1ac88ab36bcf08ef38c2e26
https://doi.org/10.54905/disssi/v27i135/e237ms2731
https://doi.org/10.54905/disssi/v27i135/e237ms2731
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 15, Iss 4, Pp ND01-ND02 (2021)
Secondary involvement of orbit in aspergillosis following paranasal sinus fungal infection is rare. A case of invasive aspergillosis of right maxillary sinus in a 31-year-old immunocompetent male patient was referred to Ophthalmology OPD with unilat
Externí odkaz:
https://doaj.org/article/65f7a16389bc4233bcec503364cc368b
Autor:
Madhumita prasad, V sachin Daigavane
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 14, Iss 9, Pp NC05-NC14 (2020)
Introduction: Phacoemulsification was introduced by Kelman in 1967. It is one of the most important innovations in ophthalmology. This has now been accepted as gold standard surgical procedure for management of cataract. Divide and conquer techniq
Externí odkaz:
https://doaj.org/article/a8278c70fc5740d6b83db252f79a59a3
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 14, Iss 2, Pp NC04-NC06 (2020)
Introduction: The most common cause of blindness is cataract, affecting over 17 million people worldwide. Cataract surgery is the most common surgical procedure done in the developed world. Aim: To study visual outcome of patients who underwent catar
Externí odkaz:
https://doaj.org/article/94bb5d5ce5ed4540878b141af8e9c4b5