Caudal duplication syndrome with unilateral hypoplasia of the pelvis and lower limb and ventriculoseptal heart defect in a mother and features of VATER association in her child

التفاصيل البيبلوغرافية
العنوان: Caudal duplication syndrome with unilateral hypoplasia of the pelvis and lower limb and ventriculoseptal heart defect in a mother and features of VATER association in her child
المؤلفون: Kristin Becker, Karol Howard, Derek Klazinga, Christine Hall
المصدر: Clinical Dysmorphology. 18:139-141
بيانات النشر: Ovid Technologies (Wolters Kluwer Health), 2009.
سنة النشر: 2009
مصطلحات موضوعية: Adult, medicine.medical_specialty, Fistula, Uterus, Pelvis, Pathology and Forensic Medicine, medicine, Humans, Abnormalities, Multiple, Genetics (clinical), Leg, business.industry, Heart Septal Defects, Syndrome, General Medicine, Labia majora, Anatomy, Intestinal Duplication, medicine.disease, Hypoplasia, Surgery, medicine.anatomical_structure, Caudal duplication, Pediatrics, Perinatology and Child Health, Female, Imperforate anus, business
الوصف: We report the case of a 22-year-old female with caudal duplication syndrome, who in addition to intestinal duplication, imperforate anus, a dydelphic uterus and a single kidney also had a ventricular septal defect and hypoplasia of the left pelvis, leg, labia majora and left side of a duplicated vagina. She gave birth to a male baby with features of the VATER association including a tracheooesophageal fistula, a ventriculoseptal defect, an atrial septal defect and mild hypospadias. We suggest that caudal duplication syndrome and the VATER association may overlap and our two cases suggest possible autosomal dominant inheritance.
تدمد: 0962-8827
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c403255a5d74e32c7fddf3550cd4e6c3
https://doi.org/10.1097/mcd.0b013e32832d0703
رقم الأكسشن: edsair.doi.dedup.....c403255a5d74e32c7fddf3550cd4e6c3
قاعدة البيانات: OpenAIRE