Fabry's disease: Difference between revisions

Jump to navigation Jump to search
No edit summary
Ghsanadgol (talk | contribs)
No edit summary
 
(6 intermediate revisions by 3 users not shown)
Line 16: Line 16:
}}
}}
{{Fabry's disease}}
{{Fabry's disease}}
{{CMG}}; {{AE}} {{AN}} {{Neepa Shah}}
{{CMG}}; {{AE}}  


{{SK}}
*


==[[Fabry's disease overview|Overview]]  ==
==[[Fabry's disease overview|Overview]]  ==
Line 46: Line 43:


==Diagnosis==
==Diagnosis==
==== [[Fabry's disease history and symptoms|History and Symptoms]] ====
*The first clinical symptoms interfering with the child's well-being and performance arise in childhood, typically between the ages of 3 and 10 years, and generally a few years later in girls than in boys
*Lack of sweating ([[anhidrosis]]) or decreased sweating
*[[Fatigue (medical)|Fatigue]]
* Red spots on skin ([[angiokeratoma]]s): tiny, painless [[papules]] that appear at any region of the body, but are predominant on the thighs, buttocks, lower abdomen, and groin.
* Burning pain of the extremities. This pain can become very intense, especially when one has a fever.
*[[Loss of vision]] or blurry vision from corneal opacities.
*[[Difficulty swallowing]] ([[dysphagia]])
*[[Abdominal pain]]
*[[Greasy stools]] ([[steatorrhea]])
*[[Chest pain]] and [[palpitations]]
*[[Delayed puberty]]
*[[Pyrexia of unknown origin]]
*[[Cyanosis]] of extremities on exposure to cold ([[Raynaud's phenomenon]])
*[[Hearing loss]]
*[[Loss of sensation]]s in extremities
*[[Telangiectasis]]
*[[Lack of coordination of muscle movement]] ([[ataxia]])
[[Fabry's disease physical examination|Physical Examination]]
[[Fabry's disease laboratory findings|Laboratory Findings]]
[[Fabry's disease electrocardiogram|Electrocardiogram]]
[[Fabry's disease CT|CT]] | [[Fabry's disease MRI|MRI]]
[[Fabry's disease echocardiography or ultrasound|Echocardiography or Ultrasound]]
[[Fabry's disease other imaging findings|Other Imaging Findings]]
[[Fabry's disease other diagnostic studies|Other Diagnostic Studies]]


==Treatment==
==Treatment==

Latest revision as of 20:07, 23 May 2022

Template:DiseaseDisorder infobox

Fabry's disease Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Fabry's disease from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

CT

MRI

Echocardiography or Ultrasound

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

Fabry's disease On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Fabry's disease

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Fabry's disease

CDC on Fabry's disease

Fabry's disease in the news

Blogs on Fabry's disease

Directions to Hospitals Treating Fabry's disease

Risk calculators and risk factors for Fabry's disease

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:


Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Fabry's disease from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Treatment

Medical Therapy | Surgery | Primary Prevention | Secondary Prevention | Cost-Effectiveness of Therapy | Future or Investigation Therapies

Case Studies

Case #1

External links

References

[1] Caterina Bartolotta, Marcello Filogamo, Paolo Colomba, Carmela Zizzo, Giuseppe Albeggiani, Simone Scalia, Daniele Francofonte, Giuseppe Cammarata, Vincenzo Savica, Giovanni Duro, FP907 HISTORY OF ANDERSON - FABRY DISEASE, Nephrology Dialysis Transplantation, Volume 30, Issue suppl_3, 1 May 2015, Page iii379, https://doi.org/10.1093/ndt/gfv186.08


[2] Eng CM, Germain DP, Banikazemi M, et al. Fabry disease: guidelines for the evaluation and management of multi-organ system involvement. Genet Med 2006;8: 539–548.

[3] Elleder M, Poupĕtová H, Kozich V . Fetal pathology in Fabry’s disease and mucopolysaccharidosis type I. Cesk Patol 1998;34:7–12.

[4] Thurberg BL, Politei JM . Histologic abnormalities of placental tissues in Fabry disease: a case report and review of the literature. Hum Pathol 2012;43:610–614. [5] Deegan PB, Baehner AF, Barba Romero MA, Hughes DA, Kampmann C, Beck M; European FOS Investigators. Natural history of Fabry disease in females in the Fabry Outcome Survey. J Med Genet. 2006 Apr;43(4):347-52. Epub 2005 Oct 14. Citation on PubMed or Free article on PubMed Central