Macroglossia: Difference between revisions
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==Overview== | ==Overview== | ||
The common causes of | The common causes of macroglossia include [[acromegaly]], [[amyloidosis]], [[beckwith-Wiedemann syndrome]], [[congenital hypothyroidism]] and [[down syndrome]]. | ||
==Causes== | ==Causes== | ||
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| '''Genetic''' | | '''Genetic''' | ||
|bgcolor="Beige"|[[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 | |bgcolor="Beige"|[[Alpha-mannosidosis]], [[Beckwith-Wiedemann syndrome]], 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]] | ||
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Latest revision as of 16:12, 28 October 2015
| Macroglossia | |
| ICD-10 | Q38.2 |
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| ICD-9 | 529.8 |
| OMIM | 153630 |
| DiseasesDB | 7689 |
| MeSH | D008260 |
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WikiDoc Resources for Macroglossia |
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Most recent articles on Macroglossia Most cited articles on Macroglossia |
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Powerpoint slides on Macroglossia |
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Evidence Based Medicine |
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Clinical Trials |
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Ongoing Trials on Macroglossia at Clinical Trials.gov Clinical Trials on Macroglossia at Google
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Guidelines / Policies / Govt |
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US National Guidelines Clearinghouse on Macroglossia
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News |
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Commentary |
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Definitions |
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Patient Resources / Community |
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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 |
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Causes & Risk Factors for Macroglossia |
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Continuing Medical Education (CME) |
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International |
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Business |
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Experimental / Informatics |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Carlos A Lopez, M.D. [2]
Overview
The common causes of macroglossia 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, Beckwith-Wiedemann syndrome, 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 |
| 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