Silver-russell syndrome following in vitro fertilization

Pediatric and Developmental Pathology

Volumn 11, Issue 4, 2008, Pages 329-331

  Douzgou, Sofia ^a   Mingarelli, Rita ^a   Tarani, Luigi ^b   De Crescenzo, Agostina ^c   Riccio, Andrea ^d  

^a CASA SOLLIEVO DELLA SOFFERENZA HOSPITAL   (Italy)

^b SAPIENZA UNIVERSITY OF ROME   (Italy)

^c SECOND UNIVERSITY OF NAPLES   (Italy)

^d INSTITUTE OF GENETICS AND BIOPHYSICS ADRIANO BUZZATI TRAVERSO   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

BECKWITH WIEDEMANN SYNDROME; FERTILIZATION IN VITRO; GENOME IMPRINTING; GROWTH RETARDATION; HUMAN; LETTER; PHYSICAL EXAMINATION; PRIORITY JOURNAL; SEROLOGY; SILVER RUSSELL SYNDROME;

ABNORMALITIES, MULTIPLE; ADULT; CHROMOSOMES, HUMAN, PAIR 11; CRANIOFACIAL ABNORMALITIES; DNA METHYLATION; FEMALE; FERTILIZATION IN VITRO; FETAL GROWTH RETARDATION; HUMANS; INFANT, NEWBORN; MALE; PREGNANCY; ULTRASONOGRAPHY, PRENATAL;

EID: 53549127260     PISSN: 10935266     EISSN: 16155742     Source Type: Journal    
DOI: 10.2350/08-04-0458.1     Document Type: Letter

References (3)

1. Lucifero D, Chaillet JR, Trasler JM. Potential significance of genomic imprinting defects for reproduction and assisted reproductive technology. Hum Reprod Update 2004;10:3-18.
2. Wollmann HA, Kirchner T, Enders H, Preece MA, Ranke MB. Growth and symptoms in Silver-Russell syndrome: review on the basis of 386 patients. Eur J Pediatr 1995;154:958-968.
3. Cerrato F, Sparago A, Verde G, et al. Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann Syndrome and Wilms' tumour. Hum Mol Genet. 2008; 17:1427-1435.