نتایج جستجو برای: macroglossia

تعداد نتایج: 373  

Journal: :Journal of medical genetics 1974
G F Smith S Sachdeva N Janakiraman S N Sinha

Armendares, S., Buentello, L., Salamanca, F., and Cantu-Garza, J. M. (1972). A dicentric Y chromosome without evidence of sex chromosomal mosaicism, 46,XYqdic, in a patient with features of Turner's syndrome. Journal of Medical Genetics, 9, 96-100. Caspersson, T., Lomakka, G., and Zech, L. (1971). The 24 fluorescence patterns of the human metaphase chromosomes-distinguishing characters and vari...

Journal: :Ear, nose, & throat journal 2005
Sandra Doria Xavier Ivo Filho Bussoloti Helena Müller

Amyloidosis is characterized by an abnormal extracellular deposition of amyloid in different tissues and organs, where it usually causes some type of dysfunction. Its cause is unknown. The two main forms of amyloidosis are systemic and localized; the latter is rare. No satisfactory treatment for systemic amyloidosis has been discovered, and mean survival is poor, ranging from 5 to 15 months dep...

Journal: :Philippine Journal of Otolaryngology-Head and Neck Surgery 2016

2006

Sir, The article by Bose and his colleagues' deserves some comment. It is certainly unusual to find an exomphalos in one of monozygotic twins, although it has been described before. To label a baby as Beckwith-Wiedemann syndrome simply on the basis of the presence of an exomphalos and a large tongue is surely, however, not justified. The essence of the syndrome is the combination of exomphalos,...

Journal: :Annali italiani di chirurgia 2016
Maria Giulia Cristofaro Walter Colangeli Umberto Riccelli Mario Giudice

UNLABELLED Lipomas are the most common benign soft tissue mesenchymal tumours composed of mature adipose tissue. They are uncommon in the oral and maxillofacial regions, with 15-20 % of cases involving the head and neck region and less than 5% of all benign oral lesions. Multiple symmetric lipomatosis is rare and characterized by diffuse growth and nonencapsulated lipomas. It is usually found i...

2006
SUDEEP SINGH Thomas

Sir, The article by Bose and his colleagues' deserves some comment. It is certainly unusual to find an exomphalos in one of monozygotic twins, although it has been described before. To label a baby as Beckwith-Wiedemann syndrome simply on the basis of the presence of an exomphalos and a large tongue is surely, however, not justified. The essence of the syndrome is the combination of exomphalos,...

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