نتایج جستجو برای: hypoglossia

تعداد نتایج: 19  

Journal: :Journal of medical genetics 1990
D Kumar

Moebius syndrome consists of congenital complete or partial facial nerve palsy with or without paralysis of other cranial nerves (most commonly an abducens paralysis) and often associated with other malformations of the limbs and orofacial structures. The first description of congenital facial diplegia was given by von Graaefe in 18801 and this was soon followed by other reports. Moebius2 3 dre...

Journal: :Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics 2008
Frederico Salles Marcos Anchieta Patrícia Costa Bezerra Maria Lúcia G M Torres Elizabeth Queiroz Jorge Faber

Aglossia is a rare anomaly caused by failed embryogenesis of the lateral lingual swellings and tuberculum impar from the fourth to eighth gestational weeks. Most cases of aglossia and hypoglossia reported in the literature were associated with limb deformities, cleft palate, deafness, situs inversus, and several syndromes, such as Moebius, Pierre Robin, and Hanhart. This report describes the ca...

2010
Renita Lorina Castelino Shishir Ram Shetty Subhas Babu G Kumuda Arvind Rao H T

The oromandibular-limb hypogenesis syndrome comprises a group of anomalies which simultaneously affect the mandible, tongue, and maxilla with or without reductive limb anomalies. It is characterized by failure of development of the intraoral region and distal extremities. Multiple and variable deformities of the mandible, maxilla and tongue may occur in combination with a variety of limb defect...

2016
Ritesh Rambharos Kalaskar Alkesh Godhane Ashita Kalaskar Swati Demble

Aglossia is a rare congenital malformation that often occurs as an isolated disorder or is observed in association with other congenital deformities, particularly limb defects. We present a unique case of a 7-year-old girl with aglossia, hypodactyli, rudimentary ears, retrognathic and V-shaped mandible. Her parental history revealed intrauterine exposure of medicines. The patient had problems i...

Journal: :Journal of medical genetics 1991
Y Gillerot L Van Maldergem R Chef L Koulischer

A stillborn female with Hanhart's syndrome in association with hydrocephalus owing to stenosis of the aqueduct of Sylvius is presented. Neuropathological findings are suggestive of an acquired pathophysiological mechanism.

Journal: :Journal of oral medicine and oral surgery 2022

Background: A positive prenatal history of maternal fever has been found to express as a range defects in infants including limb reduction, central nervous system defects, facial dysmorphogenesis and foetal death. Oromandibular hypogenesis syndrome is rare spectrum congenital disorders characterised by malformations the tongue, mandible, maxilla limbs. They present sporadic cases with extremely...

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