Macroglossia: Difference between revisions
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{{SI}} | {{SI}} | ||
{{CMG}} | {{CMG}} {{CLG}} | ||
==Overview== | ==Overview== | ||
The common causes of macroglossia include [[acromegaly]], [[amyloidosis]], [[beckwith-Wiedemann syndrome]], [[congenital hypothyroidism]] and [[down syndrome]]. | |||
==Causes== | ==Causes== | ||
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|-bgcolor="LightSteelBlue" | |-bgcolor="LightSteelBlue" | ||
| '''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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| '''Ophthalmologic''' | | '''Ophthalmologic''' | ||
|bgcolor="Beige"| | |bgcolor="Beige"| No underlying causes | ||
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| '''Psychiatric''' | | '''Psychiatric''' | ||
|bgcolor="Beige"| | |bgcolor="Beige"| No underlying causes | ||
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| '''Renal / Electrolyte''' | | '''Renal / Electrolyte''' | ||
|bgcolor="Beige"| | |bgcolor="Beige"| No underlying causes | ||
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===Causes in Alphabetical Order=== | ===Causes in Alphabetical Order=== | ||
{{columns-list|2| | |||
* 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]] | ||
}} | |||
{{Congenital malformations and deformations of digestive system}} | {{Congenital malformations and deformations of digestive system}} |
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 |
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
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