Ellis-Van Creveld Syndrome, neonatal teeth and breastfeeding impairment: a case report
نویسندگان
چکیده
ABSTRACT Because of multisystemic impairment in patients with Ellis-van Creveld syndrome, multidisciplinary care may be demanded since birth to assure breastfeeding. This report presents a case an infant that was facing breastfeeding difficulties because maxillary neonatal teeth. A 3 months old male syndrome referred Pediatric Dentistry Department two upper teeth causing difficulties. Clinical examination revealed position compatible 51 and 61, both presented uncommon ectopic soft tissue placement, conical crown hypoplastic enamel covered by large amount dental biofilm. Radiography indicated they were normal series had 2/3 completion. Due mobility impaired breastfeeding, treatment option exodontia. Early tooth eruption, such as natal teeth, itself can’t considered reason for But exodontia must when early erupted tooth(s) impairs especially systemically compromised infants. In this present report, after extraction, the able breastfeed gain weight properly.
منابع مشابه
Chondroectodermal dysplasia (Ellis-Van Creveld syndrome: A case report
Ellis-Van Creveld syndrome is a very rare congenital disorder which its principal features are polysyndactyly, chondrodysplasia, cardiac abnormalities and ectodermal dysplasia. We report a 10-year-old girl with major manifestations of this syndrome who also had multiple brownish macules and patches on trunk and extremities with aortic and pulmonary stenosis in echocardiographic evaluations.
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Ellis-van Creveld syndrome also known as chondroectodermal dysplasia or mesoectodermal dysplasia; a rare genetic disorder of the skeletal dysplasia. 'Six-fingered dwarfism' (digital integer deficiency) was an alternative designation used for this condition when it was being studied in the Amish. It is characterized by short-limb dwarfism, polydactyly, malformation of the bones of the wrist, dys...
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متن کاملEllis-Van Creveld syndrome
Ellis-van Creveld syndrome (EVC) is a chondral and ectodermal dysplasia characterized by short ribs, polydactyly, growth retardation, and ectodermal and heart defects. It is a rare disease with approximately 150 cases reported worldwide. The exact prevalence is unknown, but the syndrome seems more common among the Amish community. Prenatal abnormalities (that may be detected by ultrasound exami...
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ژورنال
عنوان ژورنال: RGO - Revista Gaúcha de Odontologia
سال: 2021
ISSN: ['0103-6971', '1981-8637']
DOI: https://doi.org/10.1590/1981-863720210004620200048