Macroglossia: Difference between revisions
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==Overview== | ==Overview== | ||
The common causes of dysuria include [[Acromegaly]], [[amyloidosis]], [[beckwith-Wiedemann syndrome]], [[congenital hypothyroidism]] and [[down syndrome]]. | |||
==Causes== | ==Causes== |
Revision as of 16:09, 28 October 2015
Macroglossia | |
ICD-10 | Q38.2 |
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ICD-9 | 529.8 |
OMIM | 153630 |
DiseasesDB | 7689 |
MeSH | D008260 |
WikiDoc Resources for Macroglossia |
Articles |
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Most recent articles on Macroglossia Most cited articles on Macroglossia |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Carlos A Lopez, M.D. [2]
Overview
The common causes of dysuria include Acromegaly, amyloidosis, beckwith-Wiedemann syndrome, congenital hypothyroidism and down syndrome.
Causes
Life Threatening Causes
Life-threatening causes include conditions which may result in death or permanent disability within 24 hours if left untreated.
Common Causes
- Acromegaly
- Amyloidosis
- Beckwith-Wiedemann syndrome
- Congenital hypothyroidism
- Down syndrome
- Hurler syndrome
- I-cell disease
Causes by Organ System
Cardiovascular | Cardiac amyloidosis |
Chemical / poisoning | No underlying causes |
Dermatologic | Hemangioma |
Drug Side Effect | Angioedema |
Ear Nose Throat | Acromegaly |
Endocrine | Acromegaly, congenital hypothyroidism, growth hormone secreting pituitary adenoma, hypothyroidism |
Environmental | No underlying causes |
Gastroenterologic | No underlying causes |
Genetic | Alpha-mannosidosis, chromosome 12p tetrasomy syndrome, chromosome 9q deletion syndrome, congenital micrognathia, down syndrome, gM1 gangliosidoses, gM3 gangliosidoses, glycogen storage disease, Hunter syndrome, Hurler syndrome, Limb-girdle muscular dystrophy, lymphoma, monoclonal gammopathy of undetermined significance, I-cell disease, omphalocele, Smith-Lemli-Opitz syndrome, Pompe disease, Potocki-Lupski syndrome, Simpson-Golabi-Behmel syndrome, tongue cancer, Beckwith-Wiedemann syndrome |
Hematologic | Multiple myeloma, monoclonal gammopathy of undetermined significance, lymphoma, down syndrome |
Iatrogenic | No underlying causes |
Infectious Disease | No underlying causes |
Musculoskeletal / Ortho | Acromegaly, Beckwith-Wiedemann syndrome, congenital hypothyroidism, cystic hygroma, Limb-girdle muscular dystrophy, multiple myeloma, sleep apnea, Simpson-Golabi-Behmel syndrome, Beckwith-Wiedemann syndrome, tongue cancer |
Neurologic | Neurofibromatosis |
Nutritional / Metabolic | Cardiac amyloidosis, amyloidosis, gM1 gangliosidoses, gM3 gangliosidoses, Hunter syndrome, immunoglobulin light chain amyloidosis, I-cell disease, Pompe disease, Potocki-Lupski syndrome |
Obstetric/Gynecologic | No underlying causes |
Oncologic | Hemangioma |
Ophthalmologic | No underlying causes |
Overdose / Toxicity | No underlying causes |
Psychiatric | No underlying causes |
Pulmonary | No underlying causes |
Renal / Electrolyte | No underlying causes |
Rheum / Immune / Allergy | Angioedema |
Sexual | No underlying causes |
Trauma | No underlying causes |
Urologic | No underlying causes |
Miscellaneous | Sleep apnea |
Causes in Alphabetical Order
Template:Congenital malformations and deformations of digestive system