X-linked Moesin Associated Immunodeficiency
Recruiting
Observational Study
Immune Deficiency
Autoimmune Diseases
Infections
Diagnosis
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 4 – 80
- Sex
- Male
- Study type
- Observational
- Participants needed
- 16 (estimated)
- Sponsor
- Institut National de la Santé Et de la Recherche Médicale, France · Government
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About This Trial
Moesin deficiency was initially described in 7 male participants aged 4 to 69 years and is characterized by lymphopenia of the 3 lineages and moderate neutropenia. Genetically, 6 out of 7 participants had the same missense mutation in the moesin gene located on the X chromosome. The 7th patient has a mutation leading to the premature introduction of a STOP codon into the protein.Clinically the 7 p…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Male patient with a mutation in the MOESIN gene (MSN)
* No objection to the collection of personal health data
Exclusion Criteria:
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Contacts