Severe nasomaxillary hypoplasia (Binder phenotype) on prenatal US/MRI: an important marker for the prenatal diagnosis of chondrodysplasia punctata
Author:
Publisher
Springer Science and Business Media LLC
Subject
Radiology Nuclear Medicine and imaging,Pediatrics, Perinatology, and Child Health
Link
http://link.springer.com/article/10.1007/s00247-018-4098-8/fulltext.html
Reference19 articles.
1. Tim-aroon T, Jaovisidha S, Wattanasirichaigoon D (2011) A new case of maternal lupus-associated chondrodysplasia punctata with extensive spinal anomalies. Am J Med Genet A 155a:1487–1491
2. Boulet S, Dieterich K, Althuser M et al (2010) Brachytelephalangic chondrodysplasia punctata: prenatal diagnosis and postnatal outcome. Fetal Diagn Ther 28:186–190
3. Chitayat D, Keating S, Zand DJ et al (2008) Chondrodysplasia punctata associated with maternal autoimmune diseases: expanding the spectrum from systemic lupus erythematosus (SLE) to mixed connective tissue disease (MCTD) and scleroderma report of eight cases. Am J Med Genet A 146a:3038–3053
4. Colin E, Touraine R, Levaillant JM et al (2012) Binder phenotype in mothers affected with autoimmune disorders. J Matern Fetal Neonat Med 25:1413–1418
5. Hertzberg BS, Kliewer MA, Decker M et al (1999) Antenatal ultrasonographic diagnosis of rhizomelic chondrodysplasia punctata. J Ultrasound Med 18:715–718
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2. Binder's syndrome: A narrative review;Special Care in Dentistry;2022-06-02
3. Fetal Flat-Facies on Prenatal Ultrasound: Is it Chondrodysplasia Punctata? A Retrospective Chart Review of 62 Fetuses;Journal of Fetal Medicine;2022-04-20
4. Surgical Treatment for Patients With Binder Syndrome, Clinical Features and Associated Symptoms;Journal of Craniofacial Surgery;2021-10-28
5. GGCX ‐related congenital combined vitamin K‐dependent clotting factors deficiency‐1: Description of a fetus with chondrodysplasia punctata;American Journal of Medical Genetics Part A;2021-09-24
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