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Hepatic Fibrosis, Congenital
Important
It is possible that the main title of the report Hepatic Fibrosis, Congenitalis not the name you expected.
Synonyms
- CHF
Disorder Subdivisions
- None
General Discussion
Congenital Hepatic Fibrosis (CHF) is a rare disease that affects both the liver and kidneys. The patient is born with this disorder (congenital), and it is inherited as an autosomal recessive trait. The typical liver abnormalities are an enlarged liver (hepatomegaly), increased pressure in the venous system that carries blood from different organs to the liver (portal hypertension), and fiber-like connective tissue that spreads over and through the liver (hepatic fibrosis), often referred to as hepatic lesions. Gastrointestinal (stomach and intestines) bleeding is frequently an early sign of this condition. Affected individuals also have impaired renal function, usually caused, in children and teenagers, by an autosomal recessive polycystic kidney disease (ARPKD). Impaired renal function associated with CHF in adults is caused by an autosomal dominant polycystic kidney disease (ADPKD).
The relationship of ARPKD to CHF is the subject of substantial controversy. Some clinicians suggest that the two conditions represent one disorder with a range of clinical/pathological presentations.
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Resources
American Kidney Fund, Inc.
6110 Executive Boulevard
Suite 1010
Rockville
MD
20852
USA
Tel: (301)881-3052
Fax: (301)881-0898
800: (800)638-8299
helpline@kideyfund.org
http://www.kidneyfund.org
American Liver Foundation
75 Maiden Lane
Suite 603
New York
NY
10038
USA
Tel: (212)668-1000
Fax: (212)483-8179
800: (800)465-4837
info@liverfoundation.org
http://www.liverfoundation.org
National Kidney Foundation
30 East 33rd Street
New York
NY
10016
Tel: (212)889-2210
Fax: (212)689-9261
800: (800)622-9010
info@kidney.org
http://www.kidney.org
NIH/National Kidney and Urologic Diseases Information Clearinghouse
3 Information Way
Bethesda
MD
20892-3580
800: (800)891-5390
nkudic@info.niddk.nih.gov
http://kidney.niddk.nih.gov/
International Patient Advocacy Association
800 Bellevue Way
MGM Building, Suite 400
Bellevue
WA
98004
Tel: (426)646-3768ARPKD/CHF Alliance
PO Box 70
Kirkwood
PA
17536
USA
Tel: (717)529-5555
Fax: (800)807-9110
800: (800)708-8892
info@arpkdchf.org
http://www.arpkdchf.org
For a Complete Report:
This is an abstract of a report from the National Organization for Rare Disorders, Inc. ® (NORD). A copy of the complete report can be obtained for a small fee by visiting the NORD website. The complete report contains additional information including symptoms, causes, affected population, related disorders, standard and investigational treatments (if available), and references from medical literature. For a full-text version of this topic, see http://www.rarediseases.org/search/rdblist.html
The information provided in this report is not intended for diagnostic purposes. It is provided for informational purposes only. NORD recommends that affected individuals seek the advice or counsel of their own personal physicians.
It is possible that the title of this topic is not the name you selected. Please check the Synonyms listing to find the alternate name(s) and Disorder Subdivision(s) covered by this report
This disease entry is based upon medical information available through the date at the end of the topic. Since NORD's resources are limited, it is not possible to keep every entry in the Rare Disease Database completely current and accurate. Please check with the agencies listed in the Resources section for the most current information about this disorder.
For additional information and assistance about rare disorders, please contact the National Organization for Rare Disorders at P.O. Box 1968, Danbury, CT 06813-1968; phone (203) 744-0100; web site www.rarediseases.org or email orphan@rarediseases.org
Last Updated: 5/18/2008
Copyright 1992, 2003 National Organization for Rare Disorders, Inc.
WebMD Medical Reference from the National Organization of Rare Disorders
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