Zobrazeno 1 - 10 of 15 pro vyhledávání: '"Rugmini Kamalammal"'
1
Akademický článek
Cow’s Milk Protein Allergy Mimicking Acrodermatitis Enteropathica
Autor: John Solomon, Rugmini Kamalammal, Mohammed Yaseen Sait, Harita Lohith
Publikováno v: Journal of Clinical and Diagnostic Research, Vol 8, Iss 3, Pp 160-161 (2014)
Cow’s milk protein allergy is an adverse immune reaction to one or more of the constituent proteins of milk obtained from any animal, most commonly alpha s 1-casein cow’s milk. In many cases, the allergy is genetic in origin. The infants may exp
Externí odkaz: https://doaj.org/article/d30667ddc34b4449aa595343bb4e29ef
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2
Akademický článek
A Case of Diamond Blackfan Anemia with Mutation in Ribosomal Protein S19
Autor: John Solomon, Rugmini Kamalammal, Godfred Antony Menezes, Mohamed Yaseen Sait, Harita Lohith, Revathy Ramalingam
Publikováno v: Journal of Clinical and Diagnostic Research, Vol 8, Iss 1, Pp 179-180 (2014)
Diamond Blackfan Anemia (DBA) is a rare disorder which presents with anemia in early infancy. This disorder is genetically and clinically heterogeneous in nature. The inheritance is mainly autosomal dominant. Approximately 25% of the cases are assoc
Externí odkaz: https://doaj.org/article/ac8d6b9d44624b779659827c91e905bc
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3
Compound heterozygous recessive thalassemia intermedia unusual presentation: a case report
Autor: Divya Narayanan Kutty, Rugmini Kamalammal
Publikováno v: Pediatric Review: International Journal of Pediatric Research. 3:798-801
About 3% of the world’s population carry β-Thalassemia genes. More than 200 mutations have been described, majority are point mutations and also some rare cases of gene deletion (17 deletions) have been reported. Those with Compound heterozygous i
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d1de644d8c988bdff734c7b903363b4c
https://doi.org/10.17511/ijpr.2016.i11.04
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4
Age stratified Seroprevalence of Cytomegalo virus in children
Autor: Rugmini Kamalammal, Balaji Balaji, Mohamed Yaseen Sait
Publikováno v: Pediatric Review: International Journal of Pediatric Research. 3:351-355
Introduction: Cytomegalovirus seroprevalance in developing countries is found to be high but there is no recent study done in India especially in children. Primary CMV infection is asymptomatic, but the virus remains latent in organs and children she
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5620774e22e85d6b79447c8580f3fd9f
https://doi.org/10.17511/ijpr.2016.i05.14
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6
Association between iron deficiency anemia and various red cell parameters with febrile convulsions in children of age group 3 to 60 months
Autor: Rugmini Kamalammal, M D Balaji
Publikováno v: International Journal of Contemporary Pediatrics. :559-562
Background: Febrile seizures are the most common seizures in children. Incidence is around 2-5% among children of age group 3-60 months. There is variable association between febrile convulsions and hematological parameters associated with iron defic
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2fb1d5a05d21003845e5e963d700f617
https://doi.org/10.18203/2349-3291.ijcp20161038
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9
Wolf–Hirschhorn syndrome
Autor: Naveen K S, Rugmini Kamalammal, Shivaprakash. N.C
Publikováno v: Pediatric Review: International Journal of Pediatric Research. 3:513-515
The Wolf–Hirschhorn syndrome (WHS) is a rare chromosomal disorder associated with a partial deletion of the short arm of chromosome 4. The major features of this disorder include a characteristic facial appearance such as a high forehead, highly ar
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8c5a5948b522114f04a3a01e7f356a83
https://doi.org/10.17511/ijpr.2016.i07.09
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10
Cholelithiasis in a neonate with Downs syndrome: a case report
Autor: Sowmya S, Rugmini Kamalammal
Publikováno v: Pediatric Review: International Journal of Pediatric Research. 3:196-198
Choleithiasis is very rare in neonates. Children with Downs syndrome are at an increased risk of developing lithiasis.There are very few reports of cholelithiasis in infants with Down’s syndrome but none in neonates. Here we report a case of Down
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2bd64fa1c5da76cd20e9d5495a9086ee
https://doi.org/10.17511/ijpr.2016.i03.10
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