Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Más filtros

Bases de datos
Asunto principal
País/Región como asunto
Tipo del documento
País de afiliación
Intervalo de año de publicación
1.
Lab Med ; 50(2): 168-173, 2019 Apr 08.
Artículo en Inglés | MEDLINE | ID: mdl-30295867

RESUMEN

BACKGROUND: The genetic background of patients with hemoglobin (Hb) H disease in Taiwan has been investigated; however, the clinical features and treatment outcomes were not reported. OBJECTIVE: To analyze the clinical features and genotypes of patients with HbH who reside in Taiwan. METHODS: We conducted a retrospective analysis of the clinical and molecular characteristics of 38 patients with HbH disease who were undergoing treatment at Kaohsiung Medical University Hospital, Taiwan. RESULTS: Initial Hb levels were lower and the numbers of patients requiring iron-chelation therapy were higher in the nondeletional HbH group than in the deletional HbH group (P <.05). Compared with the healthy population, the patients with HbH disease exhibited short body length, low body weight, and low body mass index (BMI). CONCLUSIONS: Patients with nondeletional HbH disease had lower Hb levels and a higher requirement for splenectomy and iron-chelation therapy than did those with deletional HbH disease. Also, growth status was compromised in patients with HbH disease.


Asunto(s)
Talasemia alfa , Adolescente , Adulto , Peso Corporal/fisiología , Niño , Preescolar , Femenino , Hemoglobinas/análisis , Humanos , Masculino , Persona de Mediana Edad , Estudios Retrospectivos , Esplenectomía , Taiwán/epidemiología , Adulto Joven , Talasemia alfa/complicaciones , Talasemia alfa/epidemiología , Talasemia alfa/genética , Talasemia alfa/terapia
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA