Couples with alpha-thalassaemia-1 face a 25 per cent risk of having fetuses with haemoglobin (Hb) Bart's disease. Prenatal diagnosis is conventionally performed by DNA studies of chorionic villi or amniocytes obtained from chorionic villus biopsy or amniocentesis. DNA studies are expensive and time-
Sonographic diagnosis of limb reduction defects in a fetus with haemoglobin Bart's disease at 12 weeks of gestation
β Scribed by Yung Hang Lam; Mary Hoi Yin Tang
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 176 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0197-3851
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β¦ Synopsis
Limb reduction defect is a rare event but is found in eight per cent of fetuses affected by haemoglobin Bart's disease. We present a case of haemoglobin Bart's disease with terminal transverse limb reduction defects of all four limbs diagnosed by abdominal ultrasound examination at 12 weeks of gestation. The pregnancy was terminated by suction curettage. Just prior to the procedure, transabdominal needle embryoscopy was performed and this confirmed the sonographic diagnosis. The present case demonstrates the need and feasibility of a detailed anatomic survey of a fetus affected by haemoglobin Bart's disease at 12 weeks. This is particularly relevant if the patient is considering the option of intra-uterine therapy.
π SIMILAR VOLUMES
We have studied a fetus with the prenatal sonographic diagnosis of severe nonimmune hydrops fetalis at 16 weeks of gestation, who was later shown by amniocentesis to have Down syndrome.