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Living with T-cell immunodeficiency, congenital alopecia, and nail dystrophy

A rare inherited immune condition with no working T cells, plus hair missing from birth and abnormal nails.

Understanding T-cell immunodeficiency, congenital alopecia, and nail dystrophy

T-cell immunodeficiency, congenital alopecia, and nail dystrophy is a type of severe combined immunodeficiency (SCID) that also affects hair and nails.

People lack working T cells, so they get repeated, lasting infections starting early in life, and these slow growth. They are born without scalp hair, eyebrows, or eyelashes. Nails are ridged, pitted, or curved. Brain and spinal cord differences have been described in at least two people.

Signs & symptoms

Symptoms vary from person to person. GARD lists these among the most common:

  • Repeated infections
  • Low T cell count
  • No scalp hair, eyebrows, or eyelashes
  • Ridged nails
  • Pitted nails

Not everyone has every symptom. GARD's list comes from the Human Phenotype Ontology.

Diagnosis

  1. Talk with your doctor

    Share the symptoms you've noticed, when they started and your family health history. Notes and photos can help.

  2. See a specialist

    Specialists who may be involved include allergy and immune system specialists and genetic specialists.

  3. Consider genetic testing

    Changes in FOXN1 are linked to this condition. Genetic testing and counseling can help confirm a diagnosis and explain what it means for your family.

  4. Connect with expert centers

    Immune Deficiency Foundation may keep lists of experts for this condition.

Care & treatment

Care team
Allergy and immune system specialists (allergists / immunologists); Genetic specialists (geneticists)
Expert care
Expert lists: Immune Deficiency Foundation
Treatment
GARD doesn't list specific treatments for this condition. Your care team will tailor care to your symptoms.
Research
Clinical trials and observational studies may be options. See the research section below.

General information, not medical advice. Your care team makes the decisions.

Everyday life

Living with a rare condition is easier with support.

  • Connect with Immune Deficiency Foundation
  • Keep notes on symptoms, changes and questions for appointments
  • Ask about patient registries that help research
  • Look into financial aid and travel resources for care visits
Bring these questions to your next doctor visit
What treatments can rebuild my child's immune system?
How can we lower infection risk at home?
Would FOXN1 gene testing help our family?

Quick facts

Symptoms usually startNewborn and as an Infant
InheritanceAutosomal Recessive
GenesFOXN1

Changes in the FOXN1 gene cause this condition. It is autosomal recessive, meaning a child inherits a changed copy of the gene from each parent.

Genetic

Also known as: alopecia and t-cell immunodeficiency; alopecia immunodeficiency; alymphoid cystic thymic dysgenesis; congenital alopecia and nail dystrophy associated with severe functional t-cell immunodeficiency; congenital alopecia and nail dystrophy with severe functional t-cell immunodeficiency; foxn1 deficiency

Patient organizations

Broader rare-disease groups

Source: NIH GARD · T-cell immunodeficiency, congenital alopecia, and nail dystrophyGARD ID 4358 · GARD page updated September 2026 · Plain-language summary by Know Rare; editorial review pending. General information, not medical advice.

You are more than your diagnosis

Perspectives from people navigating life with T-cell immunodeficiency, congenital alopecia, and nail dystrophy.

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