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.
Ready to participate?

Review the details below, then apply to join this clinical trial.

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
Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
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
Loading…

Loading trial locations…

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: \-
Contacts

Isabelle ANDRE, Doctor

01 42 75 43 37

isabelle.andre@inserm.fr

CONTACT