Oral findings in Robinow Syndrome: a case report in pediatric patient
نویسندگان
چکیده
منابع مشابه
Laryngeal Carcinoma in a Pediatric Patient - A Case Report
Introduction: Carcinoma of the larynx is an extremely uncommon clinical entity in pediatric age. The diagnosis of the laryngeal carcinoma is often delayed due to the low index of suspicion. The factors contributing to delayed diagnosis include the similarity of its symptoms to common benign lesions of the larynx in childhood and difficult examination of the larynx in pediatric patients. ...
متن کاملRobinow Syndrome: a Rare Case Report from a Tertiary Care Hospital in Eastern India
Background Robinow syndrome is a rare congenital disorder with phenotypically heterogeneous abnormalities. Two modes of inheritances are known for this syndrome namely autosomal recessive and autosomal dominant. Case Report We describe here an eighteen-month-old child who had mesomelic short stature, abnormal facial features, clinodactyly, micropenis and vertebral changes which were further sup...
متن کاملOral findings in Noonan syndrome: report of a case.
Oral findings in a case of Noonan syndrome in an 8-year-old Japanese male are reported. Examination of the patient revealed a narrow, high-arched palate and an anterior open bite. Cephalometric measurements showed a wide gonial angle, a large mandibular plane angle, a large Y-axis and long facial height. It is suggested that the patient had a skeletal open-bite malocclusion, which included an a...
متن کاملOral findings in Alagille syndrome. A case report.
OBJECTIVE To highlight the role of dental practitioners in the management of children with liver diseases. CLINICAL PRESENTATION A 13-year-old girl with Alagille syndrome presented with oral manifestation of end-stage liver disease that needed liver transplant. The dentition showed hypoplastic lesions and severe discoloration. The gingiva was inflamed and edematous due to poor oral hygiene an...
متن کاملA case report on autosomal recessive Robinow syndrome.
BACKGROUND Robinow syndrome or "foetal face" syndrome is an extremely rare genetic disorder with characteristic skeletal and orofacial findings. The purpose of the present case report is to describe the clinical findings of an 8 year-old female patient with autosomal recessive Robinow syndrome. CASE REPORT The patient was born to consanguineous parents and had anomalies typical of the recessi...
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ژورنال
عنوان ژورنال: Rio de Janeiro Dental Journal (Revista Científica do CRO-RJ)
سال: 2019
ISSN: 2595-4733
DOI: 10.29327/24816.4.2-7