Familial amyloidosis history and symptoms: Difference between revisions
No edit summary |
No edit summary |
||
| Line 22: | Line 22: | ||
===Common Symptoms=== | ===Common Symptoms=== | ||
Common [[symptoms]] of familial amyloidosis include:<ref name="pmid26161016">{{cite journal |vauthors=Lim AY, Lee JH, Jung KS, Gwag HB, Kim DH, Kim SJ, Lee GY, Kim JS, Kim HJ, Lee SY, Lee JE, Jeon ES, Kim K |title=Clinical features and outcomes of systemic amyloidosis with gastrointestinal involvement: a single-center experience |journal=Korean J. Intern. Med. |volume=30 |issue=4 |pages=496–505 |date=July 2015 |pmid=26161016 |pmc=4497337 |doi=10.3904/kjim.2015.30.4.496 |url=}}</ref><ref name="pmid23227278">{{cite journal |vauthors=Baker KR, Rice L |title=The amyloidoses: clinical features, diagnosis and treatment |journal=Methodist Debakey Cardiovasc J |volume=8 |issue=3 |pages=3–7 |date=2012 |pmid=23227278 |pmc=3487569 |doi= |url=}}</ref> | Common [[symptoms]] of ATTR familial amyloidosis include: | ||
* Parasthesia | |||
* Muscle weakness | |||
* Sexual problems | |||
* Constipation/ diarrhea | |||
* Urination problems | |||
* Weakness | |||
* Fatigue | |||
* Edema | |||
* Palpitation | |||
* Dizziness | |||
Common [[symptoms]] of Apolipoprotein AI familial amyloidosis include: | |||
* Parasthesia | |||
* Edema | |||
* Cutaneous lesions | |||
* Hoarseness | |||
* Cough | |||
Common [[symptoms]] of Gesolin familial amyloidosis include: | |||
* Vision problems | |||
* Droopy appearance of face, neck, and armpitt | |||
* A tingling sensation in face | |||
* Drooling or slurred speech | |||
Common [[symptoms]] of Lysozyme familial amyloidosis include: | |||
* | |||
<ref name="pmid26161016">{{cite journal |vauthors=Lim AY, Lee JH, Jung KS, Gwag HB, Kim DH, Kim SJ, Lee GY, Kim JS, Kim HJ, Lee SY, Lee JE, Jeon ES, Kim K |title=Clinical features and outcomes of systemic amyloidosis with gastrointestinal involvement: a single-center experience |journal=Korean J. Intern. Med. |volume=30 |issue=4 |pages=496–505 |date=July 2015 |pmid=26161016 |pmc=4497337 |doi=10.3904/kjim.2015.30.4.496 |url=}}</ref><ref name="pmid23227278">{{cite journal |vauthors=Baker KR, Rice L |title=The amyloidoses: clinical features, diagnosis and treatment |journal=Methodist Debakey Cardiovasc J |volume=8 |issue=3 |pages=3–7 |date=2012 |pmid=23227278 |pmc=3487569 |doi= |url=}}</ref> | |||
* [[Fatigue]] | * [[Fatigue]] | ||
* [[Weight loss]] | * [[Weight loss]] | ||
Revision as of 16:00, 11 November 2019
|
Familial amyloidosis Microchapters |
|
Diagnosis |
|---|
|
Treatment |
|
Case Studies |
|
Familial amyloidosis history and symptoms On the Web |
|
American Roentgen Ray Society Images of Familial amyloidosis history and symptoms |
|
Risk calculators and risk factors for Familial amyloidosis history and symptoms |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Farima Kahe M.D. [2]
Overview
Common symptoms of familial amyloidosis include abdominal pain, edema,enlarged tongue, skin and nail changes. Less common symptoms of amyloidosis include gastrointestinal bleeding, gross hematuria, hoarseness and paresthesias.
History and Symptoms
Common symptoms of familial amyloidosis include abdominal pain, edema and enlarged tongue. Less common symptoms of amyloidosis include gastrointestinal bleeding, gross hematuria, hoarseness and paresthesias.
History
Patients with amyloidosis may have a positive history of:[1]
- Dyspnea
- Lethargy
- Weight loss
- Chest discomfort
- Fevers or chills
- Night sweats
- Positive family history of amyloidosis
- Male gender
- African american race
Common Symptoms
Common symptoms of ATTR familial amyloidosis include:
- Parasthesia
- Muscle weakness
- Sexual problems
- Constipation/ diarrhea
- Urination problems
- Weakness
- Fatigue
- Edema
- Palpitation
- Dizziness
Common symptoms of Apolipoprotein AI familial amyloidosis include:
- Parasthesia
- Edema
- Cutaneous lesions
- Hoarseness
- Cough
Common symptoms of Gesolin familial amyloidosis include:
- Vision problems
- Droopy appearance of face, neck, and armpitt
- A tingling sensation in face
- Drooling or slurred speech
Common symptoms of Lysozyme familial amyloidosis include:
- Fatigue
- Weight loss
- Edema
- Abdominal pain
- Enlarged tongue
- Skin and nail changes
Less Common Symptoms
Less common symptoms of familial amyloidosis include:[4]
- Hoarseness
- Gastrointestinal bleeding
- Diarrhea
- Paresthesias
- Gross hematuria
- Irritative urinary symptoms
References
- ↑ Mahmood S, Palladini G, Sanchorawala V, Wechalekar A (February 2014). "Update on treatment of light chain amyloidosis". Haematologica. 99 (2): 209–21. doi:10.3324/haematol.2013.087619. PMC 3912950. PMID 24497558.
- ↑ Lim AY, Lee JH, Jung KS, Gwag HB, Kim DH, Kim SJ, Lee GY, Kim JS, Kim HJ, Lee SY, Lee JE, Jeon ES, Kim K (July 2015). "Clinical features and outcomes of systemic amyloidosis with gastrointestinal involvement: a single-center experience". Korean J. Intern. Med. 30 (4): 496–505. doi:10.3904/kjim.2015.30.4.496. PMC 4497337. PMID 26161016.
- ↑ Baker KR, Rice L (2012). "The amyloidoses: clinical features, diagnosis and treatment". Methodist Debakey Cardiovasc J. 8 (3): 3–7. PMC 3487569. PMID 23227278.
- ↑ Hamidi Asl K, Liepnieks JJ, Nakamura M, Benson MD (May 1999). "Organ-specific (localized) synthesis of Ig light chain amyloid". J. Immunol. 162 (9): 5556–60. PMID 10228037.