First trimester prenatal diagnosis of Sanfilippo disease (MPSIII) type B
- 1 January 1988
- journal article
- research article
- Published by Wiley in Prenatal Diagnosis
- Vol. 8 (1) , 47-52
- https://doi.org/10.1002/pd.1970080106
Abstract
Two pregnancies of a family at risk for Sanfilippo disease type B were monitored in the first trimester. In one case an affected fetus was diagnosed on chorionic villi by the assay of N‐acetyl‐a‐D‐glucosaminidase and confirmed on cultured fibroblasts from the aborted fetus. Pathological findings are also reported and compared with changes observed later in life. The disease was excluded in the second pregnancy.Keywords
This publication has 7 references indexed in Scilit:
- Sanfilippo disease in GreeceClinical Genetics, 1986
- FIRST TRIMESTER DIAGNOSIS OF HUNTER SYNDROME ON CHORIONIC VILLIThe Lancet, 1984
- Prenatal diagnosis of Sanfilippo disease type BHuman Genetics, 1984
- Prenatal tests for Sanfilippo disease type B in four pregnanciesPrenatal Diagnosis, 1983
- Efficient direct chromosome analyses and enzyme determinations from chorionic villi samples in the first trimester of pregnancyHuman Genetics, 1983
- Two cases of mucopolysaccharidosis type III (Sanfilippo)Acta Neuropathologica, 1979
- Sanfilippo Syndrome: Profound Deficiency of Alpha-Acetylglucosaminidase Activity in Organs and Skin Fibroblasts from Type-B PatientsProceedings of the National Academy of Sciences, 1972