Two- and three-dimensional sonographic findings of harlequin ichthyosis: case report and literature review



Document title: Two- and three-dimensional sonographic findings of harlequin ichthyosis: case report and literature review
Journal: Anais brasileiros de dermatologia
Database:
System number: 000558021
ISSN: 0365-0596
Authors: 1
2
Institutions: 1The First Affiliated Hospital Dalian Medical University, Department of Gynecology and Obstetrics, Dalian. China
2The Second Affiliated Hospital Dalian Medical University, Department of Ultrasound of Gynecology and Obstetrics, Dalian. China
Year:
Volumen: 98
Number: 6
Pages: 806-813
Country: Brasil
Language: Inglés
English abstract Background Harlequin ichthyosis (HI) is a rare skin disorder with extremely high lethality due to a mutation of the ABCA12 gene. Because of its rarity and the often-late onset, prenatal screening for HI is extremely difficult, and most pregnant women might easily miss the period for optimal examinations. Objective To summarize the sonographic features of HI for prenatal diagnostic purposes. Methods The authors describe a case of HI with no family history who was diagnosed by using prenatal ultrasound scanning. The sonographic features of HI and the clinical characteristics of pregnant women were summarized by searching relevant literature over nearly two decades. Results The unique sonographic presentations including peeling skin, clenched hands and clubfeet, ectropion, flat nose, fetal growth impairment, polyhydramnios and echogenic amniotic fluid may be primarily related to skin disorders in HI fetuses. The authors also identified a novel pathogenic ABCA12 gene mutation and explained the possible pathogenic mechanisms. Study limitations Caution should be exercised in summarizing disease characteristics because of the small number of cases, and the authors are faced with the possibility of incomplete case searching. Conclusions HI has relatively unique sonographic features. Therefore, 2D-ultrasound combined with 3D-ultrasound may be an effective method for the prenatal diagnosis of HI. Moreover, a novel pathogenic ABCA12 gene mutation may provide important clues for future research on the etiology of HI. However, the authors consider that additional studies are needed to provide more evidence for prenatal diagnosis.
Keyword: Ichthyosis,
Lamellar,
Ultrasonography,
Ultrasonography, prenatal
Full text: Texto completo (Ver HTML) Texto completo (Ver PDF)