XLA Life
XLA Life fosters the unification and empowerment of the global X-Linked Agammaglobulinemia (XLA) community through education, advocacy, and initiatives that aim to improve the overall quality of life for those affected by XLA.
SCID: Questions for your child's healthcare team
September 10, 2023
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SCID newborn screening results fact sheet
September 10, 2023
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Family planning: thinking about the future
September 10, 2023
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SCID: What healthcare providers need to know
September 10, 2023
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SCID family journey
September 10, 2023
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SCID telehealth for American Indians and Alaska Natives
September 10, 2023
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FOXN1 deficiency
Also known as nude/severe combined immunodeficiency (SCID), this rare primary immunodeficiency disrupts adaptive immunity and is characterized by congenital athymia, congenital alopecia totalis, and nail dystrophy.
International 22q11.2 Foundation
The International 22q11.2 Foundation is a nonprofit organization dedicated to supporting the needs of families and individuals affected by chromosome 22q11.2 differences by promoting awareness, state-of-the-art clinical care, cutting edge research endeavors, and solidarity with related associations around the globe.
CHARGE Syndrome Foundation
The CHARGE Syndrome Foundation champions the lifelong potential of people with CHARGE syndrome through outreach, education, and research. The CHARGE Syndrome Foundation was founded in 1982 in Columbia, Missouri. Today, the organization offers a biennial international conference, support for clinical and scientific research, and support and resources for families.
