Results 101 to 110 of about 9,359 (213)
Amyloidosis Presenting with Macroglossia
Cureus, 2018 Macroglossia is an uncommon condition that causes cosmetic and functional disabilities. We present a case of a 67-year-old patient with the past medical history of vitamin B12 deficiencies who presented with macroglossia and was found to have amyloidosis.
Shahbaz, Amir +5 more
openaire +2 more sources
BECKWITH-WIEDEMANN SYNDROME: CASE REPORT
Eurasian Journal of Medicine, 2019 A case of Beckwith-Wiedemann Syndrome is presented here in a two-month-old female with macroglossia, macrosomia, visseromegalia, anomaly of ear, umbilical hernia, and characteristically hemihypertrophy.
Vildan Ertekin +2 more
doaj
AMYLOIDOSIS AND INFLAMMATORY BOWEL DISEASE: FACT OR MITH? [PDF]
, 2017 Inflammatory Bowel Disease (IBD), which includes both Crohn's Disease (CD) and Ulcerative Colitis (UC), is a chronic idiopathic inflammatory disorder affecting the gastrointestinal tract.
Amvrosiadis, G. +13 more
core +1 more source
Obstructive sleep apnea-hypopnea syndrome (OSAHS) [PDF]
, 2009 This issue of eMedRef provides information to clinicians on the pathophysiology, diagnosis, and therapeutics of obstructive sleep apnea-hypopnea ...
Delgado, Philip, Rubeiz, Helene
core
Mandibular destructive radiolucent lesion: the first sign of multiple myeloma [PDF]
, 2016 The occurrence of a mandibular lesion as the first sign of multiple myeloma (MM) is uncommon. This report describes a case of MM diagnosed because of a mandibular lesion.
Fregnani, Eduardo Rodrigues +5 more
core +2 more sources
Primary Systemic Amyloidosis Presenting as Macroglossia
Journal of Indian Academy of Oral Medicine and Radiology, 2004 Amyloidosis is a rare disease of unknown origin characterised by extracellular deposition of fibrillar proteinaceous substance called amyloid having common morphological, structural and staining properties but variable protein composition.
Karthikeya Patil +2 more
doaj
گزارش 1 مورد تأخير تکامل به علت فوکوسيدوز همراه با ميلومننگوسل [PDF]
, 2005 فوکوسيدوز يک بيماری متابوليک ارثی نادر است که به دنبال از بين رفتن يا کمبود فعاليت آنزيم فوکوزيداز ايجاد میشود. کمبود فعاليت اين آنزيم موجب تجمع گليکواسفنگوليپيدها، گليکوپروتئينها و اليگوساکاريدهای حاوی قند فوکوز در ليزوزومهای کبد، مغز و ساير اعضا می ...
ساجدی, فیروزه +1 more
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Simpson-Golabi-Behmel syndrome types I and II [PDF]
, 2014 Simpson-Golabi-Behmel syndrome (SGBS) is a rare overgrowth syndrome clinically characterized by multiple congenital abnormalities, pre/postnatal overgrowth, distinctive craniofacial features, macrocephaly, and organomegaly.
Fernando Santos +6 more
core +1 more source
Growth pituitary adenomas: evaluation of 20 patients with surgical treatment [PDF]
, 2002 The growth hormone secreting pituitary adenomas can be mono, bi or pluri-hormonals. The most frequent association of GH is with the sub unit alpha or with the prolactin. This type of adenoma comes with the classic alterations of acromegaly, but when they
Aguiar, Paulo Henrique +3 more
core +1 more source
Management for lymphatic malformations of head and neck
Frontiers in NeurologyBackgroundTo explore the management of lymphatic malformation in head and neck.MethodsThis is a retrospective study at a single center. Data on demographic, surgery, sclerotherapy and follow-up information were collected from our Vascular Anomalies ...
Weijia Yang +5 more
doaj +1 more source