Prajnya Ranganath
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Explore the profile of Prajnya Ranganath including associated specialties, affiliations and a list of published articles.
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60
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308
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Recent Articles
1.
Garg N, Lakshmi P, Singh S, Kulshreshta S, Ranganath P, Moirangthem A, et al.
Clin Genet
. 2025 Jan;
PMID: 39806532
In 2021, the Indian Undiagnosed Diseases Program was initiated for patients without a definite diagnosis despite extensive evaluation in four participating sites. Between February 2021 and March 2023, a total...
2.
Narahari N, Kodati R, Ranganath P, Kakarla B, Gongati P
Lung India
. 2024 Oct;
41(6):464-471.
PMID: 39465929
Recurrent pulmonary infections starting from childhood often prompt evaluation for primary immunodeficiency disorders (PIDs). Hyper IgE syndrome (HIES) is a less common PID characterised by recurrent skin and pulmonary infections...
3.
Sarma A, Desai A, Rao M, Sahoo J, Shivaprasad C, Ranganath P, et al.
Horm Res Paediatr
. 2024 Jul;
:1-9.
PMID: 38986456
Introduction: Thyroid dyshormonogenesis (TDH) is a subgroup of congenital hypothyroidism with recessive inheritance resulting from disease-causing variants in thyroid hormone biosynthesis pathway genes, like DUOX2, TG, TPO, SLC5A5, SLC26A4, IYD,...
4.
Pragna Lakshmi T, Saini N, Shah M, Gowrishankar S, Dalal A, Ranganath P
Clin Genet
. 2024 Jun;
106(4):494-499.
PMID: 38860410
Variants in more than 60 different genes, most of which code for podocyte-related proteins, have been found to be associated with monogenic forms of nephrotic syndrome (NS). Biallelic variants in...
5.
Nair L, Nurul Jain J, Dalal A, Ranganath P
Pediatr Neurol
. 2024 Jan;
152:130-152.
PMID: 38277958
Background: White matter (WM) disorders with a genetic etiology are classified as leukodystrophies (LDs) and genetic leukoencephalopathies (GLEs). There are very few studies pertaining to the etiologic spectrum of these...
6.
Vanaja M, Nurul Jain J, Dalal A, Ranganath P
Indian J Med Res
. 2023 Aug;
157(6):577-590.
PMID: 37530313
Background & Objectives: Lysosomal storage disorders (LSDs) are genetic metabolic disorders which result from deficiency of lysosomal enzymes or defects in other lysosomal components. Molecular genetic testing of LSDs is...
7.
Ranganath P, Patil M
J Pediatr Genet
. 2023 Apr;
12(2):163-166.
PMID: 37090832
The "eye-of-the-tiger" sign in brain magnetic resonance imaging (MRI) is typically associated with neurodegeneration with brain iron accumulation disorders, especially pantothenate kinase-associated neurodegeneration. However, very similar neuroimaging findings may be...
8.
Sarma A, Siddardha B, T P, Ranganath P, Dalal A
J Gene Med
. 2023 Mar;
25(7):e3501.
PMID: 36942482
Background: Hereditary spastic paraplegia 81 is a recently identified, rare autosomal recessive disease, caused by biallelic pathogenic variants in the SELENOI gene, with only two families reported to date. The...
9.
Ranganath P, Dalal A
Indian Pediatr
. 2023 Mar;
60(3):177-178.
PMID: 36916356
No abstract available.
10.
John S, Gayathri K, Ahmed S, Multtani K, Menon P, Kumar R, et al.
Indian Pediatr
. 2023 Feb;
60(4):298-307.
PMID: 36814128
Justification: The diagnosis of Down syndrome (DS) is easily made clinically but the management is multi-disciplinary and life-long. There is no standard protocol available for its management in India. Process:...