Just diagnosed with Griscelli syndrome?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Griscelli syndrome, look for clinical trials, and connect with others living with it — all in one place.
Open the full interactive Griscelli syndrome hub →Overview
Griscelli syndrome is a rare condition. Also known as Chédiak-Higashi-like syndrome, Griscelli-Pruniéras syndrome, Partial albinism-immunodeficiency syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Griscelli syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:381 · OMIM 214450, 607624, 609227 · ICD-10 E70.3 · GARD 0010913
Find care for Griscelli syndrome
Authoritative references for Griscelli syndrome
Research & market landscape for Griscelli syndrome
Following Griscelli syndrome for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Griscelli syndrome — the real-world landscape behind the condition, in one place.
- Latest Griscelli syndrome research on PubMed ↗
- Recruiting Griscelli syndrome trials on ClinicalTrials.gov ↗
- Explore the Griscelli 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 Griscelli syndrome and every rare condition. See how Tomeko works with industry →
Common questions
What is Griscelli syndrome?
Griscelli syndrome is a rare condition. Also known as Chédiak-Higashi-like syndrome, Griscelli-Pruniéras syndrome, Partial albinism-immunodeficiency syndrome. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Griscelli syndrome together in one place.
What are the symptoms of Griscelli syndrome?
Symptoms of Griscelli 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 Griscelli syndrome.
How is Griscelli syndrome treated?
Treatment for Griscelli syndrome depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Griscelli syndrome, and review current options with them.
What causes Griscelli syndrome — is it genetic?
The cause and inheritance of Griscelli syndrome are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Griscelli syndrome can explain what it means for you and your family.
I was just diagnosed with Griscelli syndrome — what should I do first?
Start by learning the basics from an authoritative source, find a specialist or center that sees Griscelli syndrome, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for Griscelli syndrome?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Griscelli syndrome, filtered to your area.
Are there clinical trials for Griscelli syndrome?
Tomeko shows live, recruiting studies for Griscelli syndrome from ClinicalTrials.gov on the hub.
Related conditions
Other conditions on Tomeko you may be looking for:
- 2-aminoadipic 2-oxoadipic aciduria
- 3 beta-Hydroxysteroid dehydrogenase deficiency
- 3-hydroxy-3-methylglutaryl-CoA synthase deficiency
- 3-Hydroxyisobutyric aciduria
- 3-hydroxyisobutyryl-CoA hydrolase deficiency
- 3-methylglutaconic aciduria type 1
- 3-Methylglutaconic aciduria type 2
- 3-Methylglutaconic aciduria type 3