Just diagnosed with Isolated congenital hypoglossia/aglossia?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Isolated congenital hypoglossia/aglossia, look for clinical trials, and connect with others living with it — all in one place.
Open the full interactive Isolated congenital hypoglossia/aglossia hub →Overview
Isolated congenital hypoglossia/aglossia is a rare condition. Tomeko brings together the specialists, research, clinical trials, treatments and community for Isolated congenital hypoglossia/aglossia so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:141152 · OMIM 612776 · ICD-10 Q38.3 · GARD 0016972
Find care for Isolated congenital hypoglossia/aglossia
Authoritative references for Isolated congenital hypoglossia/aglossia
Research & market landscape for Isolated congenital hypoglossia/aglossia
Following Isolated congenital hypoglossia/aglossia for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Isolated congenital hypoglossia/aglossia — the real-world landscape behind the condition, in one place.
- Latest Isolated congenital hypoglossia/aglossia research on PubMed ↗
- Recruiting Isolated congenital hypoglossia/aglossia trials on ClinicalTrials.gov ↗
- Explore the Isolated congenital hypoglossia/aglossia research & specialist footprint on Tomeko
Researchers, patient organizations & industry: Tomeko provides de-identified, no-PHI demand and engagement signal, trial awareness, and a labeled, editorially-firewalled presence for Isolated congenital hypoglossia/aglossia and every rare condition. See how Tomeko works with industry →
Common questions
What is Isolated congenital hypoglossia/aglossia?
Isolated congenital hypoglossia/aglossia is a rare condition. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Isolated congenital hypoglossia/aglossia together in one place.
What are the symptoms of Isolated congenital hypoglossia/aglossia?
Symptoms of Isolated congenital hypoglossia/aglossia vary from person to person. For a reviewed, plain-language overview see the authoritative references below (NIH GARD, Orphanet), and discuss your own symptoms with a clinician who treats Isolated congenital hypoglossia/aglossia.
How is Isolated congenital hypoglossia/aglossia treated?
Treatment for Isolated congenital hypoglossia/aglossia depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Isolated congenital hypoglossia/aglossia, and review current options with them.
What causes Isolated congenital hypoglossia/aglossia — is it genetic?
The cause and inheritance of Isolated congenital hypoglossia/aglossia are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Isolated congenital hypoglossia/aglossia can explain what it means for you and your family.
I was just diagnosed with Isolated congenital hypoglossia/aglossia — what should I do first?
Start by learning the basics from an authoritative source, find a specialist or center that sees Isolated congenital hypoglossia/aglossia, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for Isolated congenital hypoglossia/aglossia?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Isolated congenital hypoglossia/aglossia, filtered to your area.
Are there clinical trials for Isolated congenital hypoglossia/aglossia?
Tomeko shows live, recruiting studies for Isolated congenital hypoglossia/aglossia from ClinicalTrials.gov on the hub.
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