Oromandibular-limb hypogenesis syndrome: report of a case
نویسندگان
چکیده
منابع مشابه
Oromandibular-limb Hypogenesis Syndrome Type II C: A Rare Case
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...
متن کاملOromandibular Limb Hypogenesis Syndrome Type IIB: Case Report of Hypoglossia-Hypodactyly
Hypoglossia-hypodactyly is a rare congenital anomaly affecting the tongue and the limbs. Hall in 1971 classified it under a complex group of disorders called oromandibular limb hypogenesis syndromes. It is an extremely rare condition with around 40 cases reported in the world literature. The cause of the syndrome is unknown. Some type of intrauterine trauma is the most widely accepted etiology....
متن کاملoromandibular-limb hypogenesis syndrome type ii c: a rare case
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...
متن کاملA Rare Clinical Variant of Oromandibular Limb Hypogenesis Syndrome Type I B
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...
متن کاملCraniocervical junction malformation in a child with Oromandibular-limb hypogenesis-Möbius syndrome
We report a male child with Oromandibular-limb hypogenesis (OMLH), the main features being bilateral sixth and seventh nerve palsies, limb anomalies and hypoplasia of the tongue. Additional features were shortness of the neck associated with torticollis. Radiographs of the cervical spine were non-contributory, but 3D computed tomography (CT) scanning of this area identified: a) congenital hypop...
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ژورنال
عنوان ژورنال: Japanese Journal of Oral & Maxillofacial Surgery
سال: 1984
ISSN: 2186-1579,0021-5163
DOI: 10.5794/jjoms.30.1771