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Genetics Home Reference: LEOPARD syndrome

Posted Apr 25 2011 3:56pm
Reviewed April 2011

What is LEOPARD syndrome?

LEOPARD syndrome is a condition that affects many areas of the body. The acronym LEOPARD describes the characteristic features associated with the condition: lentigines (brown skin spots similar to freckles), ECG abnormalities (measurement of abnormal electrical heart activity), ocular hypertelorism (widely spaced eyes), pulmonary stenosis (narrowing of the artery from the heart to the lungs), abnormalities of genitalia (reproductive organs), retardation of growth (short stature), and deafness. These features vary, however, even among affected individuals in the same family. Not all individuals affected with LEOPARD syndrome have all the characteristic features of this condition.

The lentigines seen in LEOPARD syndrome typically first appear in mid-childhood, mostly on the face, neck, and upper body. Affected individuals may have thousands of lentigines by the time they reach puberty. Unlike freckles, the appearance of lentigines has nothing to do with sun exposure. In addition to lentigines, people with LEOPARD syndrome may have lighter brown skin spots called café-au-lait spots. Café-au-lait spots tend to develop before the lentigines, appearing within the first year of life in most affected people.

ECG abnormalities indicate heart problems. Of the people with LEOPARD syndrome who have heart problems, about 80 percent have hypertrophic cardiomyopathy, which is a thickening of the heart muscle that forces the heart to work harder to pump blood. The hypertrophic cardiomyopathy in affected individuals most often affects the lower left chamber of the heart (the left ventricle). Up to 20 percent of people with LEOPARD syndrome that have heart problems have pulmonary stenosis.

People with LEOPARD syndrome can have a distinctive facial appearance. In addition to ocular hypertelorism, affected individuals may have droopy eyelids (ptosis), thick lips, and low-set ears.

Abnormalities of the genitalia occur most often in males with LEOPARD syndrome. The most common abnormality in affected males is undescended testes (cryptorchidism). Other males may have a urethra that opens on the underside of the penis (hypospadias). Males with LEOPARD syndrome may have a reduced ability to have biological children (decreased fertility). Females with LEOPARD syndrome may have poorly developed ovaries and delayed puberty.

At birth, people with LEOPARD syndrome are typically of normal weight and height, but in some, growth slows over time. This slow growth results in short stature in 50 to 75 percent of people with LEOPARD syndrome.

Approximately 20 percent of individuals with LEOPARD syndrome develop hearing loss. This hearing loss is caused by abnormalities in the inner ear (sensorineural deafness) and can be present from birth or develop later in life.

Other signs and symptoms of LEOPARD syndrome include learning disorders, mild developmental delay, a sunken or protruding chest, and extra folds of skin on the back of the neck.

Many of the signs and symptoms of LEOPARD syndrome also occur in a similar disorder called Noonan syndrome. It can be difficult to tell the two disorders apart in early childhood. However, the features of the two disorders differ later in life.

How common is LEOPARD syndrome?

LEOPARD syndrome is thought to be a rare condition; approximately 200 cases have been reported worldwide.

What genes are related to LEOPARD syndrome?

Mutations in the PTPN11, RAF1, or BRAF genes cause LEOPARD syndrome. Approximately 90 percent of individuals with LEOPARD syndrome have mutations in the PTPN11 gene. RAF1 and BRAF gene mutations are responsible for a total of about 10 percent of cases. A small proportion of people with LEOPARD syndrome do not have an identified mutation in any of these three genes. In these individuals, the cause of the condition is unknown.

The PTPN11, RAF1, and BRAF genes all provide instructions for making proteins that are involved in important signaling pathways needed for the proper formation of several types of tissue during development. These proteins also play roles in the regulation of cell division, cell movement, and cell differentiation (the process by which cells mature to carry out specific functions).

Mutations in the PTPN11, RAF1, or BRAF genes lead to the production of a protein that functions abnormally. This abnormal functioning impairs the protein's ability to respond to cell signals. A disruption in the regulation of systems that control cell growth and division leads to the characteristic features of LEOPARD syndrome.

Read more about the BRAF , PTPN11 , and RAF1 genes.

How do people inherit LEOPARD syndrome?

This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder.

In some cases, an affected person inherits the mutation from one affected parent. Other cases result from new mutations in the gene and occur in people with no history of the disorder in their family.

Where can I find information about diagnosis, management, or treatment of LEOPARD syndrome?

These resources address the diagnosis or management of LEOPARD syndrome and may include treatment providers.

You might also find information on the diagnosis or management of LEOPARD syndrome in Educational resources and Patient support .

To locate a healthcare provider, see How can I find a genetics professional in my area? in the Handbook.

Where can I find additional information about LEOPARD syndrome?

You may find the following resources about LEOPARD syndrome helpful. These materials are written for the general public.

You may also be interested in these resources, which are designed for healthcare professionals and researchers.

  • Gene ReviewsThis link leads to a site outside Genetics Home Reference. - Clinical summary
  • Gene Tests - DNA tests ordered by healthcare professionals (3 links)
  • PubMedThis link leads to a site outside Genetics Home Reference. - Recent literature
  • OMIM - Genetic disorder catalog (2 links)

What other names do people use for LEOPARD syndrome?

  • cardio-cutaneous syndrome
  • diffuse lentiginosis
  • lentiginosis profusa
  • Moynahan syndrome
  • multiple lentigines syndrome
  • progressive cardiomyopathic lentiginosis

For more information about naming genetic conditions, see the Genetics Home Reference Condition Naming Guidelines and How are genetic conditions and genes named? in the Handbook.

What if I still have specific questions about LEOPARD syndrome?

Where can I find general information about genetic conditions?

What glossary definitions help with understanding LEOPARD syndrome?

artery  ; autosomal  ; autosomal dominant  ; cardio-  ; cardiomyopathy  ; cell  ; cell division  ; cryptorchidism  ; cutaneous  ; developmental delay  ; differentiation  ; fertility  ; gene  ; genitalia  ; hypertelorism  ; hypertrophic  ; hypospadias  ; mutation  ; new mutation  ; ocular hypertelorism  ; ovary  ; protein  ; ptosis  ; puberty  ; pulmonary  ; pulmonary stenosis  ; sensorineural  ; short stature  ; sign  ; stature  ; stenosis  ; symptom  ; syndrome  ; testes  ; tissue  ; ventricle

You may find definitions for these and many other terms in the Genetics Home Reference Glossary .

See also Understanding Medical Terminology .

References (5 links)


The resources on this site should not be used as a substitute for professional medical care or advice. Users seeking information about a personal genetic disease, syndrome, or condition should consult with a qualified healthcare professional. See How can I find a genetics professional in my area? in the Handbook.

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