Just diagnosed with Czeizel-Losonci syndrome?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Czeizel-Losonci syndrome, look for clinical trials, and connect with others living with it — all in one place.
Open the full interactive Czeizel-Losonci syndrome hub →Overview
Czeizel-Losonci syndrome is a rare condition. Also known as Split hand with obstructive uropathy, spina bifida and diaphragmatic defects, Split hand-urinary anomalies-spina bifida syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Czeizel-Losonci syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:2437 · OMIM 183802 · ICD-10 Q87.8 · GARD 0004969
Find care for Czeizel-Losonci syndrome
Authoritative references for Czeizel-Losonci syndrome
Research & market landscape for Czeizel-Losonci syndrome
Following Czeizel-Losonci syndrome for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Czeizel-Losonci syndrome — the real-world landscape behind the condition, in one place.
- Latest Czeizel-Losonci syndrome research on PubMed ↗
- Recruiting Czeizel-Losonci syndrome trials on ClinicalTrials.gov ↗
- Explore the Czeizel-Losonci 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 Czeizel-Losonci syndrome and every rare condition. See how Tomeko works with industry →
Common questions
What is Czeizel-Losonci syndrome?
Czeizel-Losonci syndrome is a rare condition. Also known as Split hand with obstructive uropathy, spina bifida and diaphragmatic defects, Split hand-urinary anomalies-spina bifida syndrome. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Czeizel-Losonci syndrome together in one place.
What are the symptoms of Czeizel-Losonci syndrome?
Symptoms of Czeizel-Losonci 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 Czeizel-Losonci syndrome.
How is Czeizel-Losonci syndrome treated?
Treatment for Czeizel-Losonci syndrome depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Czeizel-Losonci syndrome, and review current options with them.
What causes Czeizel-Losonci syndrome — is it genetic?
The cause and inheritance of Czeizel-Losonci syndrome are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Czeizel-Losonci syndrome can explain what it means for you and your family.
I was just diagnosed with Czeizel-Losonci syndrome — what should I do first?
Start by learning the basics from an authoritative source, find a specialist or center that sees Czeizel-Losonci syndrome, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for Czeizel-Losonci syndrome?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Czeizel-Losonci syndrome, filtered to your area.
Are there clinical trials for Czeizel-Losonci syndrome?
Tomeko shows live, recruiting studies for Czeizel-Losonci syndrome from ClinicalTrials.gov on the hub.
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