Meundi Manasa Anand, Nair Gopakumar R, Sreenivasan Prathima, Raj A C
Department of Oral Medicine, Diagnosis and Radiology, Dayananda Sagar College of Dental Sciences, Shavige Malleshwara Hills, Kumaraswamy Layout, Bangalore 560078, India.
Case Rep Dent. 2013;2013:370695. doi: 10.1155/2013/370695. Epub 2013 Feb 4.
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. The characteristic features of the syndrome are hypoglossia, limb anomalies of variable degree, and micrognathia of the mandible. This unique case report of hypoglossia-hypodactyly was observed in a patient with normal mandible. In addition, patient also had pulmonary regurgitation. His parents and other siblings were normal. Positive prenatal history of maternal hyperthermia was obtained suspecting it to be the cause of the syndrome.
舌下腺发育不全-指(趾)发育不全是一种影响舌头和四肢的罕见先天性异常。1971年,霍尔将其归类于一组称为口下颌肢体发育不全综合征的复杂疾病中。这是一种极其罕见的病症,世界文献中报道的病例约有40例。该综合征的病因尚不清楚。某种类型的子宫内创伤是最被广泛接受的病因。该综合征的特征性表现为舌下腺发育不全、不同程度的肢体异常以及下颌骨小颌畸形。这例独特的舌下腺发育不全-指(趾)发育不全病例在一名下颌骨正常的患者中被观察到。此外,患者还患有肺动脉反流。他的父母和其他兄弟姐妹均正常。有母亲孕期发热的阳性产前史,怀疑这是该综合征的病因。