Zobrazeno 1 - 10 of 13 pro vyhledávání: '"Amit Vatkar"'
1
Neuromyopathy due to mitochondrial trifunctional protein deficiency caused by novel HADHA mutation
Autor: Amit Vatkar, Nishigandha Joshi, Smita Patil, Mumtaz Shariff
Publikováno v: Indian Journal of Child Health. 9:84-86
Mitochondrial trifunctional protein deficiency (MTP deficiency or MTPD) is a rare autosomal recessive disorder of oxidation of long-chain fatty acids. It is characterized by severe neonatal manifestations such as cardiomyopathy, hypoglycemia, metabol
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a687939f2c74a92b7dddcd79e00d2593
https://doi.org/10.32677/ijch.v9i5.3393
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2
Neurological manifestation of Vitamin D deficiency
Autor: Amit Vatkar, Saniya Sroa, Shweta Nair, Fehmida N
Publikováno v: Indian Journal of Case Reports. :430-432
Idiopathic intracranial hypertension, also known as pseudotumor cerebri, is a disorder with raised intracranial pressure, headache, papilledema, visual disturbances with a normal cerebrospinal fluid examination, and normal neuroimaging. It is rare in
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f23a6a6255ef8fd5871d9f9367b9f8c7
https://doi.org/10.32677/ijcr.v7i10.3100
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4
Devic’s disease – A case report
Autor: Kapil Bainade, V. Kotrashetti, Amit Vatkar, Saili Bunde, Vijay Baburao Sonawane
Publikováno v: Indian Journal of Child Health. 7:464-467
Devic disease (Neuromyelitis Optica – [NMO]) is a severe inflammatory demyelinating condition that targets astrocytes in the optic nerves and spinal cord. It is characterized by optic neuritis and transverse myelitis. The disease is very rare with
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7133af8cbf2a566efaffaac4efbacd3f
https://doi.org/10.32677/ijch.2020.v07.i11.009
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5
Compressive myelopathy presenting with paraparesis in pediatric age
Autor: Samarth Gupta, Shweta Ravindran Nair, Amit Vatkar, Kapil Bainade, Vijay Baburao Sonawane, V. Kotrashetti
Publikováno v: Pediatric Review: International Journal of Pediatric Research. 7:313-316
Compressive myelopathy is a common presentation of the adult age group secondary to degenerating etiologies. Trauma is a rare cause of compressive myelopathy, especially in the pediatric age group as the pediatric spine is more elastic than that of a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::acb028818d37ccfc623e1be043c07575
https://doi.org/10.17511/ijpr.2020.i06.14
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7
Cornelia de Lange syndrome: A rare genetic disorder
Autor: V. Kotrashetti, Amit Vatkar, Vijay BaburaoSonawane, Abolee Pansare, Kapil Bainade
Publikováno v: Pediatric Review: International Journal of Pediatric Research. 7:152-156
Cornelia de Lange Syndrome (CdLS) was first reported by Vrolik in 1849 and Brachmann in 1916, followed by Cornelia de Lange in 1933, after whom the syndrome is named. This disorder has a varied presentation but is mainly characterized by distinctive
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d840cea57db05112b09280ab22553268
https://doi.org/10.17511/ijpr.2020.i03.07
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