Gastrointestinal complications of Russell-Silver syndrome: A pilot study

American Journal of Medical Genetics

Volumn 113, Issue 1, 2002, Pages 15-19

  Anderson, Jeff ^a,d   Viskochil, David ^b   O'Gorman, Molly ^c   Gonzales, Chad ^b  

^a UNIVERSITY OF NORTH CAROLINA   (United States)

^b UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^c PRIMARY CHILDREN'S MEDICAL CENTER   (United States)

^d NONE   (United States)

Author keywords

Failure to thrive; Gastroesophageal reflux; Nissen fundoplication; Reflux esophagitis; Russell Silver syndrome

Indexed keywords

ARTICLE; CLINICAL FEATURE; ESOPHAGITIS; FACE MALFORMATION; FAILURE TO THRIVE; GASTROESOPHAGEAL REFLUX; GASTROINTESTINAL SYMPTOM; HEAD CIRCUMFERENCE; HUMAN; INTRAUTERINE GROWTH RETARDATION; MAJOR CLINICAL STUDY; POSTNATAL GROWTH; PRIORITY JOURNAL; SILVER RUSSELL SYNDROME;

ABNORMALITIES, MULTIPLE; CHROMOSOME ABERRATIONS; FEMALE; FETAL GROWTH RETARDATION; GASTROINTESTINAL DISEASES; HUMANS; INFANT, LOW BIRTH WEIGHT; INFANT, NEWBORN; PILOT PROJECTS; PREGNANCY; SYNDROME;

EID: 0037110930     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10667     Document Type: Article

References (15)

1. Blissett J, Harris G, Kirk J. 2000. Effect of growth hormone therapy on feeding problems and food intake in children with growth disorders. Acta Paediatr 89:644-649.
2. Blissett J, Harris G, Kirk J. 2001. Feeding problems in Silver-Russell syndrome. Dev Med Child Neurol 43:39-44.
3. Cazgan AL, Parano E, Pavone L, De Vivo DC. 1994. Metabolic dysfunction in Russell syndrome. J Inher Metab Dis 17:244-245.
4. Dorr S, Midro AT, Farber C, Giannakudis J, Hansmann I. 2001. Construction of a detailed physical and transcript map of the candidate region for Russell-Silver syndrome on chromosome 17q23-q24. Genomics 71:174-181.
5. Herbst JJ. 2000. Gastroesophageal reflux. In: Behrman RE, Kliegman RK, Jenson HB, editors. Nelson textbook of pediatrics. Philadelphia: WB Saunders. p 1125-1126.
6. Lai KYC, Skuse D, Tanhope R, Hindmarsh P. 1994. Cognitive abilities associated with Silver-Russell syndrome. Arch Dis Child 71:490-496.
7. Monk D, Wakeling E, Proud V, Hitchins M, Abu-Amero S, Stanier P, Preece M, et al. 2000. Duplication of 7p11.2-p13, including GRB10, in Silver-Russell syndrome. Am J Hum Genet 66:36-46.
8. Nellhaus G. 1968. Composite international and interracial graphs. Pediatrics 41:106.
9. Price SM, Stanhope R, Garrett C, Preece MA, Trembath RC. 1999. The spectrum of Silver-Russell syndrome: a clinical and molecular genetic study and new diagnostic criteria. J Med Genet 36:837-842.
10. Russell A. 1954. A syndrome of intrauterine dwarfism recognizable at birth with craniofacial dysostosis, disproportionate short arms and other anomalies. Proc R Soc Med 47:1040-1044.
11. Silver HK, Siyasu W, George J, Deamer WC. 1953. Syndrome of congenital hemihypertrophy, shortness of stature, and elevated urinary gonadotropins. Pediatrics 12:368-376.
12. Stanhope R, Albanese A, Azcona C. 1998. Growth hormone treatment of Russell-Silver syndrome. Horm Res 49(suppl 2):37-40.
13. Tanner JM, Lejarra H, Cameron N. 1975. The natural history of the Silver-Russell syndrome: a longitudinal study of thirty-nine cases. Pediatr Res 9:611-623.
14. Wakeling EL, Abu-Amero S, Price SM, Stanier P, Trembath RC, Moore GE, Preece MA. 1998. Genetics of Silver-Russell syndrome. Horm Res 49(suppl 2):32-36.
15. Wollman HA, Kirchner T, Enders H, Preece MA, Ranke MB. 1995. Growth and symptoms in Silver-Russell syndrome: review on the basis of 386 patients. Eur J Pediatr 154:958-968.