Overhydrated hereditary stomatocytosis (Q104358): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| (One intermediate revision by the same user not shown) | |||||||||||||||
| Property / Knowledge Architect | |||||||||||||||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Collection date | |||||||||||||||
16 August 2026
| |||||||||||||||
| Property / Collection date: 16 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 10:13, 17 August 2026
Overhydrated hereditary stomatocytosis is a disorder of red cell membrane permeability to monovalent cations and is characterised clinically by haemolytic anaemia. Onset occurs during the neonatal period or infancy with haemolytic anaemia that may require occasional blood transfusions. Splenomegaly or hepatosplenomegaly are present.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_595647587 |
||
| English | Overhydrated hereditary stomatocytosis |
Overhydrated hereditary stomatocytosis is a disorder of red cell membrane permeability to monovalent cations and is characterised clinically by haemolytic anaemia. Onset occurs during the neonatal period or infancy with haemolytic anaemia that may require occasional blood transfusions. Splenomegaly or hepatosplenomegaly are present. |
Statements
CID11:ID_595647587
0 references
dki-india-ID_595647587
0 references
Concluído
0 references
16 August 2026
0 references
