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Living with Steatocystoma multiplex-natal teeth syndrome

A rare genetic condition with many skin cysts and teeth that are already present at birth.

Understanding Steatocystoma multiplex-natal teeth syndrome

Steatocystoma multiplex-natal teeth syndrome is a rare genetic condition with many skin cysts and natal teeth.

People have many oil-filled skin cysts (steatocystomas) spread over the body. They also have natal teeth, which are teeth present at or soon after birth. Signs may begin in the newborn or infant years.

Signs & symptoms

GARD doesn't list specific symptoms for this condition yet. The summary describes:

  • Many skin cysts (steatocystomas)
  • Teeth present at birth (natal teeth)

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, gum, teeth and mouth specialists and skin, hair, and nail specialists.

  3. Ask which tests can help

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

Care & treatment

Care team
Genetic specialists (geneticists); Gum, teeth and mouth specialists (odontologists); Skin, hair, and nail specialists (dermatologists)
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 Children's Skin Disease 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
How should natal teeth be cared for in a baby?
What can be done about the skin cysts?
Is genetic testing available for our family?

Quick facts

Symptoms usually startNewborn and as an Infant
InheritanceAutosomal Dominant

Changes in genes (variants) cause this condition. It is autosomal dominant, meaning one changed copy of a gene can cause it. GARD doesn't list which gene.

GeneticSkin

Also known as: steatocystoma multiplex with natal teeth

Patient organizations

Broader rare-disease groups

Source: NIH GARD · Steatocystoma multiplex-natal teeth syndromeGARD ID 5004 · 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 Steatocystoma multiplex-natal teeth syndrome.

Explore the Steatocystoma multiplex-natal teeth syndrome blog

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