Just diagnosed with X-linked intellectual disability-retinitis pigmentosa syndrome?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees X-linked intellectual disability-retinitis pigmentosa syndrome, look for clinical trials, and connect with others living with it — all in one place.
Open the full interactive X-linked intellectual disability-retinitis pigmentosa syndrome hub →Overview
X-linked intellectual disability-retinitis pigmentosa syndrome is a rare condition. Also known as Aldred syndrome, Retinitis pigmentosa and intellectual disability due to Xp11.3 microdeletion, Retinitis pigmentosa and intellectual disability due to del(X)(p11.3), Retinitis pigmentosa and intellectual disability due to monosomy Xp11.3. Tomeko brings together the specialists, research, clinical trials, treatments and community for X-linked intellectual disability-retinitis pigmentosa syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:85332 · OMIM 300578 · ICD-10 H35.5 · GARD 0008360
Find care for X-linked intellectual disability-retinitis pigmentosa syndrome
- Find a specialist or center for X-linked intellectual disability-retinitis pigmentosa syndrome
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- Open the interactive X-linked intellectual disability-retinitis pigmentosa syndrome hub — care near you, live trials & community
Authoritative references for X-linked intellectual disability-retinitis pigmentosa syndrome
Research & market landscape for X-linked intellectual disability-retinitis pigmentosa syndrome
Following X-linked intellectual disability-retinitis pigmentosa syndrome for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for X-linked intellectual disability-retinitis pigmentosa syndrome — the real-world landscape behind the condition, in one place.
- Latest X-linked intellectual disability-retinitis pigmentosa syndrome research on PubMed ↗
- Recruiting X-linked intellectual disability-retinitis pigmentosa syndrome trials on ClinicalTrials.gov ↗
- Explore the X-linked intellectual disability-retinitis pigmentosa syndrome 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 X-linked intellectual disability-retinitis pigmentosa syndrome and every rare condition. See how Tomeko works with industry →
Common questions
What is X-linked intellectual disability-retinitis pigmentosa syndrome?
X-linked intellectual disability-retinitis pigmentosa syndrome is a rare condition. Also known as Aldred syndrome, Retinitis pigmentosa and intellectual disability due to Xp11.3 microdeletion, Retinitis pigmentosa and intellectual disability due to del(X)(p11.3), Retinitis pigmentosa and intellectual disability due to monosomy Xp11.3. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for X-linked intellectual disability-retinitis pigmentosa syndrome together in one place.
What are the symptoms of X-linked intellectual disability-retinitis pigmentosa syndrome?
Symptoms of X-linked intellectual disability-retinitis pigmentosa syndrome 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 X-linked intellectual disability-retinitis pigmentosa syndrome.
How is X-linked intellectual disability-retinitis pigmentosa syndrome treated?
Treatment for X-linked intellectual disability-retinitis pigmentosa syndrome depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see X-linked intellectual disability-retinitis pigmentosa syndrome, and review current options with them.
What causes X-linked intellectual disability-retinitis pigmentosa syndrome — is it genetic?
The cause and inheritance of X-linked intellectual disability-retinitis pigmentosa syndrome are described in the authoritative references linked on this page. A genetics or specialist clinician who treats X-linked intellectual disability-retinitis pigmentosa syndrome can explain what it means for you and your family.
I was just diagnosed with X-linked intellectual disability-retinitis pigmentosa syndrome — what should I do first?
Start by learning the basics from an authoritative source, find a specialist or center that sees X-linked intellectual disability-retinitis pigmentosa syndrome, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for X-linked intellectual disability-retinitis pigmentosa syndrome?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat X-linked intellectual disability-retinitis pigmentosa syndrome, filtered to your area.
Are there clinical trials for X-linked intellectual disability-retinitis pigmentosa syndrome?
Tomeko shows live, recruiting studies for X-linked intellectual disability-retinitis pigmentosa syndrome from ClinicalTrials.gov on the hub.
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