1.
J Med Genet
; 35(2): 153-6, 1998 Feb.
Article
in English
| MEDLINE
| ID: mdl-9507397
ABSTRACT
Simpson-Golabi-Behmel syndrome (SGBS) is an X linked disorder characterised by pre- and postnatal overgrowth, coarse facial features, and visceral and skeletal abnormalities. Like other overgrowth syndromes, in the SGBS there is an increased risk for developing neoplasia, mainly embryonic, such as Wilms tumour. We report a 3 year old male patient with SGBS and hepatocellular carcinoma, a previously undescribed tumour associated with the syndrome.
Subject(s)
Carcinoma, Hepatocellular/complications , Liver Neoplasms/complications , Sex Chromosome Aberrations/genetics , X Chromosome/genetics , Carcinoma, Hepatocellular/genetics , Cesarean Section , Child, Preschool , Cleft Lip/genetics , Cleft Lip/surgery , Cleft Palate/genetics , Cleft Palate/surgery , Fatal Outcome , Female , Fetal Macrosomia/genetics , Genetic Linkage , Humans , Immunohistochemistry , Infant, Premature , Lipoma/genetics , Liver/diagnostic imaging , Liver Neoplasms/genetics , Macroglossia/genetics , Male , Pregnancy , Pregnancy Complications , Syndrome , Tomography, X-Ray , Ultrasonography
2.
Arch. argent. pediatr
; 80(1): 75-9, 1982.
Article
in Spanish
| LILACS
| ID: lil-7559
3.
Arch. argent. pediatr
; 80(1): 75-9, 1982.
Article
in Spanish
| BINACIS
| ID: bin-36032
