A Rare Association of Monosomy 18P Syndrome and Polyglandular Autoimmune Syndrome Type IIIA

1. Faust J, Habedank M, Nieuwenhuijsen C. The 18 p-syndrome. Report of four cases. Eur J Pediatr. 1976; 123 (1): 59-66.10.1007/BF00497681954771Search in Google Scholar

2. Turleau C. Monosomy 18p review. Orphanet J Rare Dis. 2008; 3: 4 doi: 10.1186/1750-1172-3-4.10.1186/1750-1172-3-4226525818284672Search in Google Scholar

3. Jain N, Reitnauer PJ, Rao KW, Aylsworth AS, Calikoglu AS. Autoimmune polyendocrinopathy associated with ring chromosome 18. J Pediatr Endocrinol Metab. 2011; 24(9-10): 847-850.10.1515/JPEM.2011.32022145491Search in Google Scholar

4. Dacou-Voutetakis C, Sertedaki A, Maniatis- Christidis M, Sarri C, Karadima G, Petersen MB, et al. Insulin dependent diabetes mellitus (IDDM) and autoimmune thyroiditis in a boy with a ring chromosome 18: additional evidence of autoimmunity or IDDM gene(s) on chromosome 18. J Med Genet. 1999; 36(2): 156-158.Search in Google Scholar

5. Gluckman PD. Autoimmune thyroiditis in a case of 18p-syndrome. Aust Paediatr J. 1977; 13(2): 122-124.10.1111/j.1440-1754.1977.tb01137.x578739Search in Google Scholar

6. Martinez-Mir A, Zlotogorski A, Gordon D, Petukhova L, Mo J, Gilliam TC, et al. Genomewide scan for linkage reveals evidence of several susceptibility loci for alopecia areata. Am J Hum Genet. 2007; 80(2): 316-328.10.1086/511442178535417236136Search in Google Scholar