Definition

Nevoid basal cell carcinoma syndrome is a group of conditions passed down through families. The disorder involves the skin, nervous system, eyes, endocrine glands, urinary and reproductive systems, and bones.

It causes an unusual facial appearance and a higher risk for skin cancers and noncancerous tumors.

Alternative Names

NBCC syndrome; Gorlin syndrome; Gorlin-Goltz syndrome; Basal cell nevus syndrome (BCNS); Basal cell cancer - nevoid basal cell carcinoma syndrome

Causes

Nevoid basal cell carcinoma syndrome is a rare genetic condition. The main gene linked to the syndrome is known as PTCH (patched). A second gene, called SUFU, has also been associated with this condition.

Variations in these genes are most commonly passed down through families as an autosomal dominant trait. This means you develop the syndrome if either parent passes the gene to you. If either of your parents has this syndrome, you have a 50% chance of having it. It is also possible to develop this gene variation with no family history.

Symptoms

Main symptoms of this disorder are:

• A type of skin cancer called basal cell carcinoma that develops around the time of puberty
• A noncancerous tumor of the jaw, called keratocystic odontogenic tumor that also develops during puberty

Other symptoms include:

• Broad nose
• Cleft palate
• Heavy, protruding brow
• Jaw that sticks out (in some cases)
• Wide-set eyes
• Pitting on palms and soles

The condition may affect the nervous system and lead to:

• Eye problems
• Deafness
• Intellectual disability
• Seizures
• Tumors of the brain

The condition also leads to bone defects, including:

• Curvature of the back (scoliosis)
• Severe curvature of the back (kyphosis)
• Abnormal ribs

Exams and Tests

There may be a family history of this disorder and a past history of basal cell skin cancers.

Tests may reveal:

• Brain tumors
• Cysts in the jaw, which can lead to abnormal tooth development or jaw fractures
• Abnormalities in the colored part (iris) or lens of the eye
• Head swelling due to fluid on the brain (hydrocephalus)
• Rib abnormalities

Tests that may be done include:

• Echocardiogram (ultrasound of the heart)
• Genetic testing (in some people)
• MRI of the brain
• Skin biopsy of tumors
• X-rays of the bones, teeth, and skull
• Ultrasound to check for ovarian tumors

Treatment

It is important to get examined by a skin specialist (dermatologist) often, so that skin cancers may be treated while they are still small.

People with this disorder may also be seen and treated by other specialists, depending on which part of the body is affected. For example, a cancer specialist (oncologist) may treat tumors in the body, and an orthopedic surgeon may help treat bone problems.

Outlook (Prognosis)

Frequent follow-up with a variety of specialists is important for having a good outcome.

Possible Complications

People with this condition may develop:

• Blindness
• Brain tumor
• Deafness
• Fractures
• Ovarian tumors
• Cardiac fibromas
• Skin damage and severe scarring due to skin cancers

When to Contact a Medical Professional

Contact your health care provider if:

• You or any family members have nevoid basal cell carcinoma syndrome, especially if you are planning to have a child.
• You have a child who has symptoms of this disorder.

Prevention

Couples with a family history of this syndrome might consider genetic counseling before becoming pregnant.

Staying out of the sun and using sunscreen can help prevent new basal cell skin cancers.

Avoid radiation such as x-rays. People with this condition are very sensitive to radiation. Exposure to radiation can lead to skin cancers.

References

Epstein EH. Nevoid basal cell carcinoma syndrome (Gorlin syndrome). In: Lebwohl MG, Heymann WR, Coulson IH, Murrell DF, eds. Treatment of Skin Disease: Comprehensive Therapeutic Strategies. 6th ed. Philadelphia, PA: Elsevier; 2022:chap 170.

Martin KL. Tumors of the skin. In: Kliegman RM, St. Geme JW, Blum NJ, et al, eds. Nelson Textbook of Pediatrics. 22nd ed. Philadelphia, PA: Elsevier; 2025:chap 711.

Walsh MF, Cadoo K, Salo-Mullen EE, Dubard-Gault M, Stadler ZK, Offit K. Genetic factors: hereditary cancer predisposition syndromes. In: Niederhuber JE, Armitage JO, Kastan MB, Doroshow JH, Tepper JE, eds. Abeloff's Clinical Oncology. 6th ed. Philadelphia, PA: Elsevier; 2020:chap 13.