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Living with 46,XX testicular disorder of sex development

A condition in which people with two X chromosomes have a male appearance and small testes.

Understanding 46,XX testicular disorder of sex development

46,XX testicular disorder of sex development is a condition in which people with two X chromosomes have a male appearance.

People have male external genitalia and generally small testes. They may have undescended testes or hypospadias, and a few have genitals that are not clearly male or female. At puberty, most need testosterone treatment for male secondary sex characteristics. Hormone treatment can also help prevent breast enlargement (gynecomastia). Adults are usually shorter than average for males and are unable to have children. GARD lists onset as a variety of ages.

Signs & symptoms

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

  • Small testes
  • Genitals that are not clearly male or female (some people)
  • Low male hormone function (hypogonadism)
  • Polycystic ovaries

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 genetic specialists, hormone specialists and urinary and male reproductive system specialists.

  3. Ask which tests can help

    Your care team will decide which exams and tests can confirm the diagnosis.

  4. Connect with expert centers

    Resolve: The National Infertility Association may keep lists of experts for this condition.

Care & treatment

Care team
Genetic specialists (geneticists); Hormone specialists (endocrinologists); Urinary and male reproductive system specialists (urologists)
Expert care
Expert lists: Resolve: The National Infertility Association
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 Resolve: The National Infertility Association
  • 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
When should testosterone treatment start?
Which specialist should follow my hormones?
What are my options for fertility?

Quick facts

Symptoms usually starta variety of ages
InheritanceAutosomal Dominant

GARD says changes in genes (also called variants) cause this condition. It is listed as autosomal dominant.

GeneticEndocrineUrinary and Reproductive

Also known as: 46,xx gonadal dysgenesis; 46,xx testicular differences of sex development; 46,xx testicular disorders of sex development; 46,xx testicular dsd; de la chapelle syndrome; xx male syndrome

Patient organizations

Broader rare-disease groups

Source: NIH GARD · 46,XX testicular disorder of sex developmentGARD ID 399 · 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

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