Macroglossia: Difference between revisions
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===Causes in Alphabetical Order=== | ===Causes in Alphabetical Order=== | ||
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* 17q21.31 duplication syndrome | * 17q21.31 duplication syndrome | ||
* 22q11.2 duplication syndrome | * 22q11.2 duplication syndrome | ||
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*[[Simpson-Golabi-Behmel syndrome]] | *[[Simpson-Golabi-Behmel syndrome]] | ||
*[[Tongue cancer]] | *[[Tongue cancer]] | ||
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Revision as of 16:02, 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 |
Media |
Powerpoint slides on Macroglossia |
Evidence Based Medicine |
Clinical Trials |
Ongoing Trials on Macroglossia at Clinical Trials.gov Clinical Trials on Macroglossia at Google
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Guidelines / Policies / Govt |
US National Guidelines Clearinghouse on Macroglossia
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Books |
News |
Commentary |
Definitions |
Patient Resources / Community |
Patient resources on Macroglossia Discussion groups on Macroglossia Patient Handouts on Macroglossia Directions to Hospitals Treating Macroglossia Risk calculators and risk factors for Macroglossia
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Healthcare Provider Resources |
Causes & Risk Factors for Macroglossia |
Continuing Medical Education (CME) |
International |
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Business |
Experimental / Informatics |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Carlos A Lopez, M.D. [2]
Overview
Macroglossia is the medical term for unusual enlargement (hypertrophy) of the tongue. Severe enlargement of the tongue can cause cosmetic and functional difficulties including in speaking, eating, swallowing and sleeping.
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