What syndrome is this?

Pediatric Dermatology

Volumn 17, Issue 4, 2000, Pages 319-321

  Bishop, P R ^a   Nowicki, M J ^a   Parker, P H ^a  

^a UNIVERSITY OF MISSISSIPPI SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CLINICAL FEATURE; COLON POLYP; COLONOSCOPY; FAMILIAL POLYPOSIS; HUMAN; MALE; PENIS DISEASE; PRIORITY JOURNAL; RUVALCABA MYRHE SMITH SYNDROME; SYNDROME DELINEATION; COLON TUMOR; DIFFERENTIAL DIAGNOSIS; PATHOLOGY; PENIS; PIGMENT DISORDER; SYNDROME;

CHILD; COLONIC NEOPLASMS; COLONIC POLYPS; DIAGNOSIS, DIFFERENTIAL; HUMANS; MALE; PENIS; PIGMENTATION DISORDERS; SYNDROME;

EID: 0034219967     PISSN: 07368046     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1525-1470.2000.01787.x     Document Type: Article

References (11)

1. Hereditary gastrointestinal polyposis syndromes
2. Sotos syndrome with intestinal polyposis and pigmentary changes of the genitalia
3. Ruvalcaba-Myhre-Smith syndrome: A case with probable autosomal-dominant inheritance and additional manifestations
4. Bannayan-Riley-Ruvalaba syndrome: Remaining three formerly recognized syndromes as one etiologic entity
5. Ruvalcaba-Myhre-Smith syndrome: A new consideration in the differential diagnosis of intestinal polyposis
6. A new lipid storage myopathy observed in individuals with Ruvalcaba-Myhre-Smith syndrome
7. Dominantly inherited megalencephaly, muscle weakness, and myoliposis: A carnitine-deficient myopathy within the spectrum of the Ruvalcaba-Myhre-Smith syndrome
8. Common deletion of chromosome 10q23-24 in juvenile polyposis coli and Bannayan-Riley-Ruvalcaba syndrome
9. A juvenile polyposis tumor suppressor locus at 10q22 is deleted from nonepithelial cells in the lamina propria
10. Clinical and dermatologic aspects of the hereditary intestinal polyposes
11. Intestinal polyps