Just diagnosed with MMEP syndrome?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees MMEP syndrome, look for clinical trials, and connect with others living with it — all in one place.
Open the full interactive MMEP syndrome hub →Overview
MMEP syndrome is a rare condition. Also known as MCOPS8, Microcephaly-microphthalmia-ectrodactyly of lower limbs-prognathism syndrome, Syndromic microphthalmia type 8, Viljoen-Smart syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for MMEP syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:3434 · OMIM 601349 · ICD-10 Q87.8 · GARD 0003693
Find care for MMEP syndrome
Authoritative references for MMEP syndrome
Research & market landscape for MMEP syndrome
Following MMEP syndrome for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for MMEP syndrome — the real-world landscape behind the condition, in one place.
- Latest MMEP syndrome research on PubMed ↗
- Recruiting MMEP syndrome trials on ClinicalTrials.gov ↗
- Explore the MMEP 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 MMEP syndrome and every rare condition. See how Tomeko works with industry →
Common questions
What is MMEP syndrome?
MMEP syndrome is a rare condition. Also known as MCOPS8, Microcephaly-microphthalmia-ectrodactyly of lower limbs-prognathism syndrome, Syndromic microphthalmia type 8, Viljoen-Smart syndrome. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for MMEP syndrome together in one place.
What are the symptoms of MMEP syndrome?
Symptoms of MMEP 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 MMEP syndrome.
How is MMEP syndrome treated?
Treatment for MMEP syndrome depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see MMEP syndrome, and review current options with them.
What causes MMEP syndrome — is it genetic?
The cause and inheritance of MMEP syndrome are described in the authoritative references linked on this page. A genetics or specialist clinician who treats MMEP syndrome can explain what it means for you and your family.
I was just diagnosed with MMEP syndrome — what should I do first?
Start by learning the basics from an authoritative source, find a specialist or center that sees MMEP syndrome, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for MMEP syndrome?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat MMEP syndrome, filtered to your area.
Are there clinical trials for MMEP syndrome?
Tomeko shows live, recruiting studies for MMEP syndrome from ClinicalTrials.gov on the hub.
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