Bannayan–Riley–Ruvalcaba syndrome

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Bannayan–Riley–Ruvalcaba syndrome
Synonyms Bannayan–Zonana syndrome, Riley–Smith syndrome, Ruvalcaba–Myhre–Smith syndrome
Pronounce
Specialty Medical genetics
Symptoms Macrocephaly, lipomas, hemangiomas, pigmented macules on the glans penis
Complications N/A
Onset Childhood
Duration Lifelong
Types N/A
Causes Mutations in the PTEN gene
Risks
Diagnosis Genetic testing, clinical evaluation
Differential diagnosis Cowden syndrome, Proteus syndrome, Neurofibromatosis type I
Prevention
Treatment Symptomatic treatment, surgical removal of lipomas
Medication
Prognosis Generally good with management
Frequency Rare
Deaths


Bannayan–Riley–Ruvalcaba syndrome
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Bannayan–Riley–Ruvalcaba syndrome

Bannayan–Riley–Ruvalcaba syndrome (BRRS) is a rare overgrowth syndrome and hamartomatous disorder with a wide spectrum of phenotypic expression. It is characterized by macrocephaly, intestinal polyposis, lipomas, and pigmented macules of the glans penis.

Signs and Symptoms[edit]

BRRS is characterized by a variety of symptoms, including macrocephaly, intestinal polyposis, lipomas, and pigmented macules of the glans penis. Other symptoms may include developmental delay, thyroid problems, and an increased risk of certain types of cancer.

Causes[edit]

BRRS is caused by mutations in the PTEN gene. This gene provides instructions for making a protein that is involved in cell signaling and regulation of cell growth. Mutations in the PTEN gene disrupt the protein's function, leading to uncontrolled cell growth and division.

Diagnosis[edit]

Diagnosis of BRRS is based on clinical features and can be confirmed by genetic testing for mutations in the PTEN gene.

Treatment[edit]

Treatment for BRRS is symptomatic and supportive. It may include regular monitoring for the development of tumors and other complications.

Prognosis[edit]

The prognosis for individuals with BRRS varies. Some individuals may have mild symptoms and a normal lifespan, while others may have severe complications and a shortened lifespan.

See Also[edit]

References[edit]

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