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Proteus syndrome: Clinical profile of six patients and review of literature.
Indian J Hum Genet ; 2013 Apr; 19(2): 202-206
Article in English | IMSEAR | ID: sea-149430
ABSTRACT

OBJECTIVE:

Proteus syndrome (PS) is characterized by patchy or segmental overgrowth and hyperplasia of multiple tissues and organs, along with susceptibility to development of tumors. Very few cases are reported in literature from developing countries. Due to certain overlapping features with other overgrowth syndromes, diagnosis is usually delayed. Our aim was to describe clinical profile of this rare condition in six patients. MATERIALS AND

METHODS:

Retrospective case sheet review of patients followed in a Pediatric Genetic and Metabolic clinic at a tertiary care institute of North India with a diagnosis of hemihypertrophy/overgrowth syndrome.

RESULTS:

Six cases presented with asymmetric overgrowth and peculiar features suggestive of PS were included in this study. Age at presentation was 2 months to 10 years; two were males and four were females. Hemihypertrophy was noticed in only one case at birth, and focal overgrowths in rest of other patients were seen later during childhood.

CONCLUSION:

Due to certain overlapping features with other overgrowth syndromes, diagnosis of PS is usually delayed. Pediatricians are the first persons who come across such patients and they should be aware about this rare condition.
Subject(s)

Full text: Available Index: IMSEAR (South-East Asia) Main subject: Female / Humans / Male / Child, Preschool / Proteus Syndrome / Limb Deformities, Congenital / Fingers / Hamartoma / Hypertrophy / Infant Language: English Journal: Indian J Hum Genet Year: 2013 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Female / Humans / Male / Child, Preschool / Proteus Syndrome / Limb Deformities, Congenital / Fingers / Hamartoma / Hypertrophy / Infant Language: English Journal: Indian J Hum Genet Year: 2013 Type: Article