scholarly journals An Еducational Pеrspеctivе on Indian Infant Hеalth: Thе Еffеcts of Еducation Lеvеls on Birth Outcomе

2022 ◽  
Author(s):  
Hаng Nguyеn ◽  
Kien Le ◽  
My Nguyеn
Keyword(s):  

Abstract: Thе purposе of this study is to sее if Indian mothеrs with grеatеr lеvеls of еducation producе hеalthiеr infants (N=342,734). According to thе findings, Indian mothеrs with a highеr еducational lеvеl had hеalthiеr infants than Indian mothеrs with a lowеr еducational lеvеl. In tеrms of statistics, onе additional еducation yеar in India is linkеd to a 8.5816 gram risе in Indian birth wеight and a 0.46 pеrcеntagе point rеduction in Indian low birth wеight risk.

2018 ◽  
Vol 35 (2) ◽  
pp. 399-401 ◽  
Author(s):  
R. Devendra ◽  
P. Warang ◽  
V. Gupta ◽  
A. Chiddarwar ◽  
P. Kedar ◽  
...  
Keyword(s):  

Hemoglobin ◽  
2020 ◽  
Vol 44 (4) ◽  
pp. 297-301
Author(s):  
Jordyn A. Moore ◽  
Beverley M. Pullon ◽  
Kylie M. Drake ◽  
Stephen O. Brennan
Keyword(s):  

1983 ◽  
Vol 36 (4) ◽  
pp. 447-448 ◽  
Author(s):  
M.N. Christophorou ◽  
Polyxeni Nicolaidou
Keyword(s):  

1989 ◽  
Vol 78 (1) ◽  
pp. 152-156 ◽  
Author(s):  
M. WEISS ◽  
J. MULLER-HOCKER ◽  
B. WIEBECKE ◽  
B. H. BELOHRADSKY

2011 ◽  
Vol 85 (2) ◽  
pp. 221-224 ◽  
Author(s):  
Archana Verma ◽  
Nirmal Kumar ◽  
Veerle Lejon ◽  
Rajat Garg ◽  
Archna Sharma ◽  
...  

1987 ◽  
Vol 66 (10) ◽  
pp. 1043???1045 ◽  
Author(s):  
Ann G. Bailey ◽  
Edmond C. Bloch

2018 ◽  
Vol 08 (02) ◽  
pp. 081-085 ◽  
Author(s):  
Akella Radha Rama Devi ◽  
Srilatha Kadali ◽  
Ananthaneni Radhika ◽  
Vineeta Singh ◽  
M. Kumar ◽  
...  

AbstractThis is the first reported case of prosaposin (PSAP) mutation from India manifesting as an acute neuronal Gaucher disease-like condition. A 2-month-old male baby presented with encephalopathy, resistant tonic–clonic seizures, moderate hepatosplenomegaly, hypotonia, and cherry red spot in the retinae. The child had anemia, thrombocytopenia, elevated chitotriosidase, and normal activity of acid sphingomyelinase and low normal activity of β-glucosidase 1 (β-glucocerebrosidase 1, GBA). The child succumbed in the fourth month of life due to persistent respiratory distress and refractory seizures. The clinical phenotype, cherry red spots, elevated chitotriosidase, and lysosomal assays led to the suspicion of Gaucher disease. Exome sequencing revealed a homozygous stop codon mutation in the PSAP gene (c.G1228T, p.Glu410ter). Prenatal diagnosis in the next pregnancy revealed a carrier fetus, who was unaffected postnatally. The diagnosis of specific activator deficiency such as saposin C and saposin D deficiency (in the current study) should be considered and tested for when Gaucher disease is suspected in an infant with partially deficient or near normal GBA activity.


2015 ◽  
Vol 09 (02) ◽  
pp. 251-253 ◽  
Author(s):  
Ramesh Konanki ◽  
Suvasini Sharma ◽  
Ajay Garg ◽  
Madhulika Kabra ◽  
Sheffali Gulati
Keyword(s):  

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