نتایج جستجو برای: orofacial malformation

تعداد نتایج: 19226  

Journal: :مجله علوم اعصاب شفای خاتم 0
pouya ghaderi islamic azad university, mashhad branch, mashhad, iran mahshad abdolmaleki islamic azad university, tabriz branch, tabriz, iran negar ghasemi islamic azad university, tabriz branch, tabriz, iran bita abdolahi islamic azad university, tabriz branch, tabriz, iran

mothers exposed to antiepileptic drugs (aeds) are at high risk to born babies with orofacial malformations such as cleft lips. about 9 percent of congenital abnormalities in babies of mothers with epilepsy relates to orofacial abnormalities. maintaining safe antiepileptic drugs for millions of mothers with epilepsy is very important. researches show that new aeds have less side effects than the...

2012
Muhammad Qasim Mahmood Shaukat

The popliteal pterygium syndrome is a congenital malformation that includes orofacial, musculoskeletal and genitourinary anomalies. It is a rare autosomal dominant disorder. We report one family with popliteal pterygium syndrome affecting father and his two daughters, who underwent surgical corrections for multiple congenital malformations.

Journal: :Pediatric dentistry 1989
R J Berkowitz P Neuman P Spalding L Novak S Strandjord P F Coccia

Multimodal cancer therapy for pediatric head and neck tumors may be associated with significant developmental orofacial morbidity. This report details these effects in a child (C.I.) diagnosed at 2.5 years of age with a rhabdomyosarcoma, primary to the left buccinator. This case is of interest as C.I. has an unaffected identical twin (D.I.) for comparative study. Both were assessed by comparing...

2015
Liliana Arias Urueña Ignacio Briceño Balcazar Julio Martinez Lozano Andrew Collins Daniel Alfredo Uricoechea Patiño

OBJECTIVES To present descriptive epidemiology of Orofacial Clefts and to determine the association of syndromic forms with antenatal high-risk conditions, preterm birth, and comorbidities among nested-series of cases. METHODS A study of nested-series of cases was conducted. Frequencies of cleft type, associated congenital anomalies, syndromic, non-syndromic and multiple malformation forms, a...

2010
Hercílio MARTELLI-JÚNIOR Roseli Teixeira de MIRANDA Cassandro Moreira FERNANDES Paulo Rogério Ferreti BONAN Lívia Máris Ribeiro PARANAÍBA Edgard GRANER Ricardo D. COLETTA

OBJECTIVES Goldenhar syndrome (GS) is a relatively common developmental disorder characterized by craniofacial anomalies in association with vertebral, cardiac, renal, and central nervous system defects. This paper describes GS features with special emphasis on oral characteristics. MATERIAL AND METHODS The clinical features of 6 patients with GS aged 3 months to 12 years are described, and a...

Journal: :International Journal of Immunopathology and Pharmacology 2011

Journal: :Revista medica de Chile 2010
Julio Nazer María Constanza Ramírez Lucía Cifuentes

BACKGROUND Orofacial clefts are common and have a great medical and social importance. The Latin American Study of Congenital Malformations (ECLAMC), has maintained an epidemiological surveillance of congenital malformations since 1969, allowing the evaluation of trends in the prevalence of malformations. AIM To evaluate the evolution curve of prevalence rates of orofacial clefts from 1971 to...

2014
Ilham Ratbi Nawfal Fejjal Marie Legendre Nathalie Collot Serge Amselem Abdelaziz Sefiani

INTRODUCTION Popliteal pterygium syndrome is a congenital malformation that includes orofacial, musculoskeletal and genitourinary anomalies. It is a rare autosomal dominant disorder due to a mutation of the IRF6 gene on 1q32.2. CASE PRESENTATION A one-month-old Moroccan baby boy was diagnosed with typical features of popliteal pterygium syndrome and carried the c.250C>T; p.Arg84Cys mutation o...

Journal: :Journal of dentistry for children 2007
Lizandra Ferrari Guimarães Maria Elisa Janini Aurea Simone Barroso Vieira Lucianne Cople Maia Laura Guimarães Primo

Moebius syndrome (MS) is a rare disorder mainly characterized by bi- or unilateral palsy of the facial and abducens nerves. Among the various orofacial characteristics related to this syndrome, the following are pointed out, difficulty with sucking, tongue malformation, mandibular hypoplasia, saliva drooling, arched palate and micrognathia. In spite of the diversity of oral features described f...

Journal: :European journal of paediatric dentistry : official journal of European Academy of Paediatric Dentistry 2009
N Eronat D Cogulu F Ozkinay

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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