Noonan syndrome and systemic lupus erythematosus: Presentation in childhood

Clinical Dysmorphology

Volumn 13, Issue 3, 2004, Pages 161-163

  Alanay, Yasemin ^a   Balci, Sevim ^a   Ozen, Seza ^a  

^a HACETTEPE UNIVERSITY   (Turkey)

Author keywords

Autoimmune diseases; Noonan syndrome; Short stature; Systemic lupus erythematosus; Thrombocytopenia

Indexed keywords

ANTIHYPERTENSIVE AGENT; CALCITONIN; CALCIUM; CAPTOPRIL; HYDROXYCHLOROQUINE; PENICILLIN G; PREDNISONE; SALICYLIC ACID; VITAMIN D;

ARTHRITIS; ARTICLE; AUTOIMMUNE DISEASE; CASE REPORT; CHILDHOOD DISEASE; CONGENITAL HEART MALFORMATION; DISEASE ASSOCIATION; FACIES; HUMAN; MALE; NOONAN SYNDROME; PRIORITY JOURNAL; SCHOOL CHILD; SHORT STATURE; SYSTEMIC LUPUS ERYTHEMATOSUS; THROMBOCYTOPENIA; CHILD; KARYOTYPING; PHENOTYPE;

AUTOIMMUNE DISEASES; CHILD; FACIES; HUMANS; KARYOTYPING; LUPUS ERYTHEMATOSUS, SYSTEMIC; MALE; NOONAN SYNDROME; PHENOTYPE;

EID: 14844347691     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/01.mcd.0000127467.04018.6d     Document Type: Article

References (15)

1. Alarcon-Riquelme ME, Prokunina L (2003). Finding genes for SLE: complex interactions and complex populations. J Autoimmun 21:117-120.
2. Amoroso A, Garzia P, Vadacca M, Galluzo S, Del Porto F, Mitterhofer AP, et al. (2003). The unusual association of three autoimmune diseases in a patient with Noonan syndrome. J Adolesc Health 32:94-97.
3. Bertola DR, Sugayama SMM, Albano LMJ, Kim CA, Gonzalez CH (1999). Noonan syndrome: a clinical and genetic study of 31 patients. Rev Hosp Clin Fac Med Sao Paulo 54:147-150.
4. Evans DGR, Lonsdale RN, Patton MA (1991). Cutaneous lymphangioma and amegakaryocytic thrombocytopenia in Noonan syndrome. Clin Genet 39:228-232.
5. Martin DM, Gencyuz CF, Petty EM (2001). Systemic lupus erythematosus in a man with Noonan syndrome. Am J Med Genet 102:59-62.
6. Mendez HMM, Opitz JM (1985). Noonan syndrome: a review. Am J Med Genet 21:493-506.
7. Noonan J (1968). Hypertelorism with Turner phenotype. Am J Dis Child 116:373-380.
8. Noonan JA, Ehmke DA (1963). Associated noncardiac malformations in children with congenital heart disease. J Pediatr 63:468-470.
9. Nora JJ, Nora AH, Sinha AK (1974). The Ullrich-Noonan syndrome (Turner phenotype). Am J Dis Child 127:48-55.
10. Ranke MB, Heidemann P, Knupfer C, Enders H, Schmaltz AA, Bierich JR (1988). Noonan syndrome: growth and clinical manifestations in 144 cases. Eur J Pediatr 148:220-227.
11. Sharland M, Burch M, McKenna WM, Patton MA (1992a). A clinical study of Noonan syndrome. Arch Dis Child 67:178-183.
12. Sharland M, Patton MA, Talbot S, Chitolie A, Bevan DH (1992b). Coagulation-factor deficiencies and abnormal bleeding in Noonan's syndrome. Lancet 339:19-21.
13. Svensson J, Carsson A, Ericsson UB, Westphal O, Ivarsson SA (2003). Noonan's syndrome and autoimmune diseases. J Ped Endocrinol Metab 16:217-218.
14. Tartaglia M, Mehler EL, Goldberg R, Zampino G, Brunner HG, Kremer H, et al. (2001). Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome. Nat Genet 29:465-468.
15. Vesterhus P, Aarskog D (1973). Noonan's syndrome and autoimmune thyroiditis. J Pediatr 83:237-240.