Results 91 to 100 of about 26,761 (285)

Etiology and Outcome of Hydrops Fetalis

open access: yesPediatrics & Neonatology, 2014
The term hydrops fetalis (HF) describes generalized subcutaneous edema in the fetus or neonate, characterized by a generalized skin thickness of >5 mm. It is usually accompanied by ascites and often by pleural and/or pericardial effusion. Generally, there are two categories of HF: isoimmume and nonimmune.
openaire   +4 more sources

Genetic and clinical features of hemoglobin H disease in Chinese patients [PDF]

open access: yes, 2000
Background. Normally, one pair of each of the two α-globin genes, α1 and α2, resides on each copy of chromosome 16. In hemoglobin H disease, three of these four α-globin genes are affected by a deletion, a mutation, or both.
Chan, TK   +7 more
core   +1 more source

High diagnosis rate for nonimmune hydrops fetalis with prenatal clinical exome from the Hydrops-Yielding Diagnostic Results of Prenatal Sequencing (HYDROPS) Study

open access: yesGenetics in Medicine, 2021
H. Al-Kouatly   +11 more
semanticscholar   +1 more source

Outcomes and morbidities of patients who survive haemoglobin Bart's hydrops fetalis syndrome: 20-year retrospective review.

open access: yesHong Kong medical journal = Xianggang yi xue za zhi, 2018
INTRODUCTION Haemoglobin Bart's hydrops fetalis syndrome was once considered a fatal condition. However, advances over the past two decades have enabled survival of affected patients.
Wilson YK Chan   +5 more
semanticscholar   +1 more source

Prenatal diagnosis of thalassemia [PDF]

open access: yes, 2008
published_or_final_versio
Chan, V   +3 more
core  

Human phenotypes caused by PIEZO1 mutations; one gene, two overlapping phenotypes? [PDF]

open access: yes, 2018
PIEZO1 is a large mechanosensitive ion channel protein. Diseases associated with PIEZO1 include autosomal recessive Generalised Lymphatic Dysplasia of Fotiou (GLDF) and autosomal dominant Dehydrated Hereditary Stomatocytosis with or without ...
Albuisson   +30 more
core   +1 more source

An international registry of survivors with Hb Bart's hydrops fetalis syndrome.

open access: yesBlood, 2017
Hemoglobin (Hb) Bart's hydrops fetalis syndrome (BHFS) resulting from α0-thalassemia is considered a universally fatal disorder. However, over the last 3 decades, improvements in intrauterine interventions and perinatal intensive care have resulted in ...
D. Songdej, C. Babbs, D. Higgs
semanticscholar   +1 more source

Recurrent second-trimester intrauterine fetal death due to undiagnosed atrioventricular block: A case report [PDF]

open access: yes, 2017
Fetal cardiac abnormalities are one of the common causes of non-immune fetal hydrops. Early diagnosis and treatment may prevent the late consequences that can occur as heart failure and intrauterine fetal death. Herein we report the case of a 32-year-old
Abbas, Ahmed M.   +2 more
core   +1 more source

Analysis of Non-Immune Hyrops Fetalis: Evaluation of 15 Cases

open access: yesGynecology Obstetrics & Reproductive Medicine, 2012
OBJECTIVES: To evaluation the ultrasound characteristics, etiological factors and perinatal outcome in hydrops fetalis. STUDY DESIGN: A total of 15 hydrops fetalis presented in our perinatology unit, were studied prospectively.
Turhan Aran   +2 more
doaj  

Prenatal Diagnosis of Congenital Cystic Adenomatoid Malformations: Evolution and Outcome

open access: yesTaiwanese Journal of Obstetrics & Gynecology, 2009
Objective: The aim of this study was to describe the natural history and outcomes of fetal congenital cystic adenomatoid malformation (CCAM) of the lung in three antenatally diagnosed cases.
Wei-Shiu Chen   +3 more
doaj   +1 more source

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