Prenatal diagnosis of harlequin ichthyosis
- 23 April 1980
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 17 (4) , 275-280
- https://doi.org/10.1111/j.1399-0004.1980.tb00147.x
Abstract
The successful prenatal diagnosis of ichthyosis in the fetus of a woman whose previous liveborn child was affected with harlequin ichthyosis is reported. The fetal diagnosis was established through analysis of ultrasonographically guided fetoscopic skin biopsies. These biopsies showed premature hyperkeratosis, most marked around hair follicles and sweat ducts, and forming plugs of hyperkeratotic debris. These observations were in distinct contrast to those in control fetuses, whose epidermis consists of squamous epithelium only a few cells in depth with minimal keratinization. [The affected fetus was aborted].Keywords
This publication has 13 references indexed in Scilit:
- Prenatal Diagnosis of Classic HemophiliaNew England Journal of Medicine, 1979
- Prenatal Diagnosis of Chronic Granulomatous DiseaseNew England Journal of Medicine, 1979
- Prenatal Diagnosis of Chondroectodermal Dysplasia (Ellis-Van Creveld Syndrome) with Fetoscopy and UltrasoundNew England Journal of Medicine, 1977
- Prenatal Diagnosis of HemoglobinopathiesNew England Journal of Medicine, 1976
- The “fetoscope”—A new clinical tool for prenatal genetic diagnosisAmerican Journal of Obstetrics and Gynecology, 1975
- In Utero Diagnosis of HemoglobinopathiesNew England Journal of Medicine, 1974
- New method of intrauterine evaluation by the combined use of fetoscopy and ultrasoundAmerican Journal of Obstetrics and Gynecology, 1974
- The Structural Proteins of Harlequin Fetus: Stratum CorneumJournal of Investigative Dermatology, 1973
- Endoamnioscopy and fetal biopsy: A new techniqueAmerican Journal of Obstetrics and Gynecology, 1972