Learn About Autosomal Recessive Cutis Laxa Type 1

Condition 101 content is not available at this time, but we are continually updating the site. Please check back.

However, there may be experts who have treated this or similar conditions in our Find a Doctor section and research may be available in our Latest Advances section.

Who are the top Autosomal Recessive Cutis Laxa Type 1 Local Doctors?
Distinguished
Highly rated in
5
conditions

Institute For Medical Genetics And Human Genetics

Berlin, BE, DE 10117

Bjorn Fischer is in Berlin, Germany. Fischer is rated as a Distinguished expert by MediFind in the treatment of Autosomal Recessive Cutis Laxa Type 1. They are also highly rated in 5 other conditions, according to our data. Their top areas of expertise are De Barsy Syndrome, Autosomal Recessive Cutis Laxa Type 1, Cutis Laxa, and Wrinkly Skin Syndrome.

Distinguished
Highly rated in
33
conditions

Institute For Medical Genetics And Human Genetics

Goettingen, NI, DE 

Uwe Kornak is in Goettingen, Germany. Kornak is rated as a Distinguished expert by MediFind in the treatment of Autosomal Recessive Cutis Laxa Type 1. He is also highly rated in 33 other conditions, according to our data. His top areas of expertise are Cutis Laxa, Wrinkly Skin Syndrome, Autosomal Recessive Cutis Laxa Type 1, and Gerodermia Osteodysplastica.

 
 
 
 
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Distinguished
Highly rated in
51
conditions

Max Planck Institute For Molecular Genetics

Berlin, BE, DE 

Stefan Mundlos is in Berlin, Germany. Mundlos is rated as a Distinguished expert by MediFind in the treatment of Autosomal Recessive Cutis Laxa Type 1. He is also highly rated in 51 other conditions, according to our data. His top areas of expertise are Brachydactyly, Liebenberg Syndrome, Multiple Synostoses Syndrome 1, and Learman Syndrome.

What are the Latest Advances for Autosomal Recessive Cutis Laxa Type 1?
Loss of zebrafish atp6v1e1b, encoding a subunit of vacuolar ATPase, recapitulates human ARCL type 2C syndrome and identifies multiple pathobiological signatures.
SPG9A with the new occurrence of an ALDH18A1 mutation in a CMT1A family with PMP22 duplication: case report.
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New insight into clinical heterogeneity and inheritance diversity of FBLN5-related cutis laxa.
What are the latest Autosomal Recessive Cutis Laxa Type 1 Clinical Trials?
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