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Article

Clinicohematological and Genetic Profile of Hereditary Spherocytosis in Children: An Experience From a North Indian Center.

Journal of pediatric hematology/oncology - 1 Jul 2026

Chakraborty Ankita, Kalra Manas, Sachdeva Anupam, Kotwal Jyoti, Langer Sabina, Saraf Amrita, Rana Pallavi, Dahiya Surbhi, Arya Vandana, Aggarwal Satish, Prasad Alpana

Abstract excerpt

BACKGROUND: Hereditary spherocytosis (HS) is a genetically and clinically diverse red cell membrane disorder, with limited clinical and molecular data on pediatric patients from India. METHODS: This ambispective study, conducted at a North Indian tertiary center over a period of 6 years, evaluated HS patients for clinical, laboratory, genetic, and treatment outcomes. RESULTS: Forty-seven patients (33 males, 14...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 42054241
DOI: 10.1097/MPH.0000000000003205

Genes

ANK1
CDA
EPB42
PKLR
SLC4A1
SPTA1
SPTB

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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