Ahmed Sarar Mohamed
Biographic Data
| ID | 8259244 |
|---|---|
| NAME | Ahmed Sarar Mohamed |
| GIVEN NAMES | Ahmed Sarar |
| FAMILY NAME | Mohamed |
| SIGNATURE | MOHAMED A S |
| AFFILIATIONS | National University |
| ORCID | 0009-0009-6316-4882 |
| VERIFIED | Yes |
| TOTAL WORKS | 1 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 1 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2022 |
| LATEST PUBLICATION YEAR | 2022 |
| H-INDEX | 0 |
A Niemann–Pick Disease Type C2 with Severe Pulmonary Involvement and Limited Therapeutic Options
Niemann-Pick disease type C (NPC) is an autosomal recessive lipid storage disorder. There are two types, NPC1, which is the predominant form (95%), and the rare NPC2, which represents less than 5% of the reported cases. Niemann-Pick disease type C2 usually presents with respiratory symptoms, cholestasis, neurological impairment, and hepatosplenomegaly. Case report: Here, we report a 3-year-old boy who presented to our hospital with exacerbation o…
No prominent works on this page.
A Niemann–Pick Disease Type C2 with Severe Pulmonary Involvement and Limited Therapeutic Options
Niemann-Pick disease type C (NPC) is an autosomal recessive lipid storage disorder. There are two types, NPC1, which is the predominant form (95%), and the rare NPC2, which represents less than 5% of the reported cases. Niemann-Pick disease type C2 usually presents with respiratory symptoms, cholestasis, neurological impairment, and hepatosplenomegaly. Case report: Here, we report a 3-year-old boy who presented to our hospital with exacerbation o…
Autoimmune and Inflammatory Disorders Research (1 work) · Bronchoalveolar lavage (1 work) · Child Nutrition and Feeding Issues (1 work) · Disease (1 work) · Hepatosplenomegaly (1 work) · Hypotonia (1 work) · Internal Medicine (1 work) · Lung (1 work) · Lysosomal Storage Disorders Research (1 work) · Medicine (1 work)