M Juneja… - Fetal & Pediatric Pathology, 2011 - informahealthcare.com ... Arch Surg 44:164, 1942. Fink HA. Retention cyst of the tongue (glossocele). Oral Surg Oral Med Oral Pathol 16:1290–1293, 1963. Shear M. Cysts of the Oral Regions, 3rd ed Stoneham, MA: Butterworth-Heinemann Ltd., 205–210, 1992. ... Related articles - All 2 versions
AJ Cowan, M Skinner, JL Berk, JM Sloan… - Amyloid, 2011 - informahealthcare.com AL amyloidosis and transthyretin (ATTR) amyloidosis are the most frequent forms of systemic amyloidosis diagnosed in the United States. Macroglossia is considered to be a pathognomonic feature of AL amyloidosis. We report on two cases of systemic amyloidosis with ... Related articles - All 2 versions
C Li, C O'Gorman, RS Prather… - Reproduction, fertility, …, 2011 - ncbi.nlm.nih.gov Beckwith-Wiedeman Syndrome (BWS) is a loss of imprinting (LOI) condition that is associated with macroglossia, midline abdominal defects, and neonatal gigantism among other symptoms. These symptoms have also been seen in animals produced by SCNT. A ...
PC Hettinger… - Annals of Plastic Surgery, 2011 - journals.lww.com Wolters Kluwer Health may email you for journal alerts and information, but is committed to maintaining your privacy and will not share your personal information without your express consent. For more information, please refer to our Privacy Policy. ... Skip Navigation Links Home > ... All 3 versions
J Zou, K Yu, W Xun, X Zou, X Qu… - Oral Surgery, Oral …, 2011 - ooooe.net Received 18 March 2010; received in revised form 8 October 2010; accepted 21 October 2010. published online 04 February 2011. ... No abstract is available. To read the body of this article, please view the Full Text online. ... Visit SciVerse ScienceDirect to see if you have ... Related articles - Cached - All 4 versions
[HTML] from nih.govHS Malhotra, R Juyal, KP Malhotra… - Annals of Indian …, 2011 - ncbi.nlm.nih.gov Macroglossia is rare in patients of Duchenne muscular dystrophy (DMD), and its occurrence without any endocrinologic abnormality, seizures or an abnormal karyotype is even rarer. We describe a patient of DMD with isolated macroglossia with 271 bp deletion in exon 50 of ... Related articles - All 4 versions