Two Unusual Cases of Haemoglobin Bart's Hydrops Fetalis due to Uniparental Disomy or Non-Paternity

No abstract is available for this paper.

• Publication year

  2013

• Venue

  Fetal Diagnosis and Therapy

• Publication date

  2013-09-14

• Fields of study

  Medicine

• Identifiers
  DOI 10.1159/000354808PMID 24051347
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• ISUOG Clinical Standards Committee. Practice guidelines for performance of the routine mi-trimester fetal ultrasound scan.

  2011cited by this paper
• Re-emergence of late presentations of fetal haemoglobin Bart's disease in Hong Kong.

  2011cited by this paper
• Practice guidelines for performance of the routine mid‐trimester fetal ultrasound scan

  2011cited by this paper
• Complexity of alpha thalassemia: growing health problem with new approaches to screening, diagnosis, and therapy

  2010cited by this paper
• Assessing discrepant findings between QF‐PCR on uncultured prenatal samples and karyotyping on long‐term culture

  2009cited by this paper
• Maternal uniparental disomy of chromosome 16 resulting in hemoglobin Bart’s hydrops fetalis

  2008cited by this paper
• Incidental Discovery of Nonpaternity during Prenatal Testing of Genetic Disease

  2008cited by this paper
• A new strategy for prenatal diagnosis of homozygous α0‐thalassemia

  2006cited by this paper
• A new strategy for prenatal diagnosis of homozygous alpha(0)-thalassemia.

  2006cited by this paper
• Non-Invasive Fetal RHD Exon 7 and Exon 10 Genotyping Using Real-Time PCR Testing of Fetal DNA in Maternal Plasma

  2005cited by this paper
• Sensitivity and specificity of mean corpuscular volume testing for screening for α‐thalassemia‐1 and β‐thalassemia traits

  2005cited by this paper
• Sensitivity and specificity of mean corpuscular volume testing for screening for alpha-thalassemia-1 and beta-thalassemia traits.

  2005cited by this paper
• Cost‐effectiveness of prenatal screening for thalassaemia in Hong Kong

  2004cited by this paper
• Thalassemia screening based on red cell indices in the Chinese.

  2001cited by this paper
• Single-tube multiplex-PCR screen for common deletional determinants of α-thalassemia

  2000cited by this paper
• Single-tube multiplex-PCR screen for common deletional determinants of alpha-thalassemia.

  2000cited by this paper
• Hydrops Fetalis Caused by α-Thalassemia: An Emerging Health Care Problem

  1998cited by this paper
• Hydrops fetalis caused by alpha-thalassemia: an emerging health care problem.

  1998cited by this paper
• Prevalence and genotypes of α- and β-thalassemia carriers in Hong Kong : Implications for population screening

  1997cited by this paper
• Prevalence and genotypes of alpha‐ and beta‐thalassemia carriers in Hong Kong — Implications for population screening

  1997cited by this paper
• Uniparental disomy: a novel mechanism for thalassemia major.

  1992cited by this paper
• Uniparental disomy: a novel mechanism for thalassemia major [letter]

  1992cited by this paper
• Homozygous alpha-thalassaemia: clinical presentation, diagnosis and management. A review of 46 cases.

  1985cited by this paper
• Homozygous α‐thalassaemia: clinical presentation, diagnosis and management. A review of 46 cases

  1985cited by this paper

• Hb Bart’s Disease Due to Uniparental Disomy for Chromosome 16: The Need for Clinical Vigilance in Hydropic Fetuses with Only One Parent Carrying α0-Thalassemia

  2025cites this paper
• Misdiagnosis of Hb Bart’s disease: prenatal screening and diagnosis of thalassemia in special population

  2023cites this paper
• Characterisation of two unusual cases of haemoglobin Bart’s hydrops foetalis caused by –SEA and large novel α-globin gene cluster deletions

  2021cites this paper
• A Rare Case of Hemoglobin Bart’s Hydrops Fetalis due to Uniparental Disomy of Chromosome 16

  2021cites this paper
• Prenatal Screening for Thalassemias

  2020cites this paper
• The pitfall of antenatal thalassaemia screening

  2017cites this paper
• Prenatal ultrasound monitoring of homozygous α0-thalassemia-induced fetal anemia.

  2017cites this paper
• An international registry of survivors with Hb Bart's hydrops fetalis syndrome.

  2017cites this paper
• Fetal Heart Size

  2016cites this paper
• An Unusual Hydrops Fetalis Associated with Compound Heterozygosity for Krüppel-like Factor 1 mutations

  2016cites this paper
• A Fetus with Hb Bart’s Disease Due to Maternal Uniparental Disomy for Chromosome 16

  2016cites this paper
• Whole-Genome Array CGH Evaluation for Replacing Prenatal Karyotyping in Hong Kong

  2014cites this paper
• Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locus

  2014cites this paper