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Living with Congenital temporomandibular joint ankylosis

A rare jaw condition present from birth in which the jaw joint is stiff and the mouth opens very little.

Understanding Congenital temporomandibular joint ankylosis

Congenital temporomandibular joint ankylosis is a rare jaw condition in which the mouth opens much less than usual, without an injury or infection to explain it.

The opening can range from a few millimeters to a few centimeters. People may have facial differences, such as a jaw and chin that shift to one side, an uneven lower face, and a small jaw, along with a bad bite. They typically have feeding and breathing difficulties. Developmental delay, low muscle tone, and seizures have also been reported.

Signs & symptoms

GARD doesn't list specific symptoms for this condition yet. Its summary mentions these:

  • Limited mouth opening
  • Feeding difficulties
  • Breathing difficulties
  • Small or shifted jaw (micrognathia)
  • Bad bite (dental malocclusion)
  • Uneven lower face

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

    Your doctor may refer you to a specialist who knows rare conditions.

  3. Ask which tests can help

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

Care & treatment

Care team
A doctor familiar with rare conditions, plus specialists as needed
Expert care
Ask about multidisciplinary care centers for rare conditions
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 TMJ Association, Ltd.
  • 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
How limited is the jaw opening, and how does it affect feeding and breathing?
What surgical or other options might help?
Which specialists, such as jaw surgeons, should be on the team?

Quick facts

GARD doesn't describe a cause for this condition yet.

Also known as: congenital ankylosis of temporomandibular joint; congenital trismus

Patient organizations

Source: NIH GARD · Congenital temporomandibular joint ankylosisGARD ID 20450 · 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 Congenital temporomandibular joint ankylosis.

Explore the Congenital temporomandibular joint ankylosis blog

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  • Eligibility is confirmed by the study team

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