National Center for Advancing and Translational Sciences Genetic and Rare Diseases Information Center, a program of the National Center for Advancing and Translational Sciences

Dandy-Walker cyst with Renal-Hepatic-Pancreatic dysplasia



Other Names:
Meckel syndrome type 7; Meckel-like syndrome type 1; Meckel syndrome 7; Meckel syndrome type 7; Meckel-like syndrome type 1; Meckel syndrome 7; NPHP3-related Meckel-like syndrome; Goldston syndrome; Renal-hepatic-pancreatic dysplasia-Dandy-Walker cysts syndrome See More
Categories:

The following summary is from Orphanet, a European reference portal for information on rare diseases and orphan drugs.
orphanet

Orpha Number: 3032

Definition
NPHP3-related Meckel-like syndrome is a rare, genetic, syndromic renal malformation characterized by cystic renal dysplasia with or without prenatal oligohydramnios, central nervous system abnormalities (commonly Dandy-Walker malformation), congenital hepatic fibrosis, and absence of polydactyly.

Visit the Orphanet disease page for more resources.
Last updated: 7/1/2018

This table lists symptoms that people with this disease may have. For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed. This information comes from a database called the Human Phenotype Ontology (HPO) . The HPO collects information on symptoms that have been described in medical resources. The HPO is updated regularly. Use the HPO ID to access more in-depth information about a symptom.

Showing of 30 |
Medical Terms Other Names
Learn More:
HPO ID
80%-99% of people have these symptoms
Dandy-Walker malformation 0001305
Multicystic kidney dysplasia 0000003
Renal dysplasia 0000110
30%-79% of people have these symptoms
Abnormal biliary tract morphology 0012440
Abnormal liver parenchyma morphology 0030146
Abnormality of the pancreas 0001732
Intestinal malrotation 0002566
Oligohydramnios
Low levels of amniotic fluid
0001562
Polyhydramnios
High levels of amniotic fluid
0001561
Pulmonary hypoplasia
Small lung
Underdeveloped lung
[ more ]
0002089
1%-4% of people have these symptoms
Aortic valve stenosis
Narrowing of aortic valve
0001650
Atrial septal defect
An opening in the wall separating the top two chambers of the heart
Hole in heart wall separating two upper heart chambers
[ more ]
0001631
Biliary cirrhosis 0002613
Cholestasis
Slowed or blocked flow of bile from liver
0001396
Choroid plexus cyst 0002190
Hepatosplenomegaly
Enlarged liver and spleen
0001433
High forehead 0000348
Hypertonia 0001276
Inguinal hernia 0000023
Large fontanelles
Wide fontanelles
0000239
Multiple glomerular cysts 0100611
Pancreatic cysts 0001737
Patent ductus arteriosus 0001643
Portal hypertension 0001409
Postaxial foot polydactyly
Extra toe attached near the little toe
0001830
Right ventricular hypertrophy 0001667
Situs inversus totalis
All organs on wrong side of body
0001696
Stage 5 chronic kidney disease 0003774
Percent of people who have these symptoms is not available through HPO
Autosomal recessive inheritance 0000007
Bile duct proliferation 0001408
Showing of 30 |
Last updated: 7/1/2020

Making a diagnosis for a genetic or rare disease can often be challenging. Healthcare professionals typically look at a person’s medical history, symptoms, physical exam, and laboratory test results in order to make a diagnosis. The following resources provide information relating to diagnosis and testing for this condition. If you have questions about getting a diagnosis, you should contact a healthcare professional.

Testing Resources

  • The Genetic Testing Registry (GTR) provides information about the genetic tests for this condition. The intended audience for the GTR is health care providers and researchers. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.

If you need medical advice, you can look for doctors or other healthcare professionals who have experience with this disease. You may find these specialists through advocacy organizations, clinical trials, or articles published in medical journals. You may also want to contact a university or tertiary medical center in your area, because these centers tend to see more complex cases and have the latest technology and treatments.

If you can’t find a specialist in your local area, try contacting national or international specialists. They may be able to refer you to someone they know through conferences or research efforts. Some specialists may be willing to consult with you or your local doctors over the phone or by email if you can't travel to them for care.

You can find more tips in our guide, How to Find a Disease Specialist. We also encourage you to explore the rest of this page to find resources that can help you find specialists.

Healthcare Resources


These resources provide more information about this condition or associated symptoms. The in-depth resources contain medical and scientific language that may be hard to understand. You may want to review these resources with a medical professional.

In-Depth Information

  • The Monarch Initiative brings together data about this condition from humans and other species to help physicians and biomedical researchers. Monarch’s tools are designed to make it easier to compare the signs and symptoms (phenotypes) of different diseases and discover common features. This initiative is a collaboration between several academic institutions across the world and is funded by the National Institutes of Health. Visit the website to explore the biology of this condition.
  • Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine. 
  • Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
  • PubMed is a searchable database of medical literature and lists journal articles that discuss Dandy-Walker cyst with Renal-Hepatic-Pancreatic dysplasia. Click on the link to view a sample search on this topic.

Questions sent to GARD may be posted here if the information could be helpful to others. We remove all identifying information when posting a question to protect your privacy. If you do not want your question posted, please let us know.