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Autosomal recessive cutis laxa type 1

Just diagnosed with Autosomal recessive cutis laxa type 1?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Autosomal recessive cutis laxa type 1, look for clinical trials, and connect with others living with it — all in one place.

Open the full Autosomal recessive cutis laxa type 1 hub →

Overview

Autosomal recessive cutis laxa type 1 is a rare condition. Also known as ARCL1, Autosomal recessive cutis laxa with severe systemic involvement, Autosomal recessive cutis laxa, pulmonary emphysema type. Tomeko brings together the specialists, research, clinical trials, treatments and community for Autosomal recessive cutis laxa type 1 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:90349 · OMIM 219100, 614437, 619446 · ICD-10 Q82.8 · GARD 0008480

Find care for Autosomal recessive cutis laxa type 1

Authoritative references for Autosomal recessive cutis laxa type 1

Common questions

I was just diagnosed with Autosomal recessive cutis laxa type 1 — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Autosomal recessive cutis laxa type 1, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Autosomal recessive cutis laxa type 1?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Autosomal recessive cutis laxa type 1, filtered to your area.

Are there clinical trials for Autosomal recessive cutis laxa type 1?

Tomeko shows live, recruiting studies for Autosomal recessive cutis laxa type 1 from ClinicalTrials.gov on the hub.

Informational only — not medical advice. Always consult a qualified clinician. Provider and reference data from public sources (NIH GARD, Orphanet, OMIM, HPO, MONDO, ClinicalTrials.gov, CMS NPPES). © Tomeko · tomekohealth.com