Autosomal recessive cutis laxa type 1

Last reviewed

🖨 Print for my doctorAdvocacy Hub →
ORPHA:90349OMIM:614437Q82.8
Who is this for?
Show terms as
1Specialists8Treatment centers

Where are you in your journey?

UniteRare data is sourced from FDA.gov, ClinicalTrials.gov, Orphanet, OMIM, and NORD.
Report missing data

Overview

Also known as:

Clinical phenotype terms— hover any for plain English:

EmphysemaHP:0002097DermatochalasisHP:0010750Fragmented elastic fibers in the dermisHP:0025167Lack of skin elasticityHP:0100679PneumothoraxHP:0002107Abnormal cheek morphologyHP:0004426Peripheral pulmonary artery stenosisHP:0004969Abnormal systemic arterial morphologyHP:0011004
Orphanet ↗OMIM ↗NORD ↗

Treatments

No FDA-approved treatments are currently listed for Autosomal recessive cutis laxa type 1.

View clinical trials →

No actively recruiting trials found for Autosomal recessive cutis laxa type 1 at this time.

New trials open frequently. Follow this disease to get notified.

Search ClinicalTrials.gov ↗Join the Autosomal recessive cutis laxa type 1 community →

Specialists

1 foundView all specialists →

Treatment Centers

8 centers
🏥 NORD

Baylor College of Medicine Rare Disease Center

Baylor College of Medicine

📍 Houston, TX

🏥 NORD

Stanford Medicine Rare Disease Center

Stanford Medicine

📍 Stanford, CA

🔬 UDN

NIH Clinical Center Undiagnosed Diseases Program

National Institutes of Health

📍 Bethesda, MD

🔬 UDN

UCLA UDN Clinical Site

UCLA Health

📍 Los Angeles, CA

🔬 UDN

Baylor College of Medicine UDN Clinical Site

Baylor College of Medicine

📍 Houston, TX

🔬 UDN

Harvard/MGH UDN Clinical Site

Massachusetts General Hospital

📍 Boston, MA

🏥 NORD

Mayo Clinic Center for Individualized Medicine

Mayo Clinic

📍 Rochester, MN

👤 Mayo Clinic Center for Individualized Medicine

🏥 NORD

UCLA Rare Disease Day Program

UCLA Health

📍 Los Angeles, CA

Travel Grants

No travel grants are currently matched to Autosomal recessive cutis laxa type 1.

Search all travel grants →NORD Financial Assistance ↗

Community

Open Autosomal recessive cutis laxa type 1Forum →

No community posts yet. Be the first to share your experience with Autosomal recessive cutis laxa type 1.

Start the conversation →

Latest news about Autosomal recessive cutis laxa type 1

No recent news articles for Autosomal recessive cutis laxa type 1.

Follow this condition to be notified when news becomes available.

Caregiver Resources

NORD Caregiver Resources

Support, advocacy, and financial assistance for caregivers of rare disease patients.

Mental Health Support

Rare disease caregiving can be isolating. Connect with counseling and peer support.

Family & Caregiver Grants

Financial assistance programs specifically for caregivers of rare disease patients.

Social Security Disability

Learn how rare disease patients may qualify for SSDI/SSI benefits.

Common questions about Autosomal recessive cutis laxa type 1

Which specialists treat Autosomal recessive cutis laxa type 1?

1 specialists and care centers treating Autosomal recessive cutis laxa type 1 are listed on UniteRare, sourced from ClinicalTrials.gov principal investigators, published research, and the NPPES NPI registry.