Niemann-Pick Disease: An Underdiagnosed Lysosomal Storage Disorder
Lysosomal storage disorders (LSDs) collectively constitute a significant public health burden in developing countries. Commoner LSDs include Gaucher, Fabry, and Niemann-Pick disease (NPD), but many cases remain undiagnosed. With the high incidence of consanguineous marriages, South East Asian countr...
Saved in:
Main Authors: | Inusha Panigrahi, Manoj Dhanorkar, Renu Suthar, Chanchal Kumar, Mullai Baalaaji, Babu Ram Thapa, Jasvinder Kalra |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2019-01-01
|
Series: | Case Reports in Genetics |
Online Access: | http://dx.doi.org/10.1155/2019/3108093 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Fatal Postpartum Hemorrhage in a Patient with Niemann-Pick Disease Type B
by: Atakan Tanacan, et al.
Published: (2018-01-01) -
Stress and anxiety among caregivers of adult patients with Niemann-Pick Type C disease
by: Izabela Dawidowska-Nowak, et al.
Published: (2024-12-01) -
Corrigendum to “Niemann-Pick Disease Type C Presenting as a Developmental Coordination Disorder with Bullying by Peers in a School-Age Child”
by: Ryo Suzuki, et al.
Published: (2017-01-01) -
Endothelial and neuronal engagement by AAV-BR1 gene therapy alleviates neurological symptoms and lipid deposition in a mouse model of Niemann-Pick type C2
by: Charlotte Laurfelt Munch Rasmussen, et al.
Published: (2025-01-01) -
Changes in glycosphingolipid levels in plasma and cerebrospinal fluid of individuals with Lysosomal Free Sialic Acid Storage Disorder
by: Marya S. Sabir, et al.
Published: (2025-01-01)