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Hoyeraal-Hreidarsson Syndrome due to PARN Mutations: Fourteen Years of Follow-Up

2015; Elsevier BV; Volume: 56; Linguagem: Inglês

10.1016/j.pediatrneurol.2015.12.005

1873-5150

Ashley Burris, Bari J. Ballew, Joshua B. Kentosh, Clesson Turner, Scott A. Norton, Neelam Giri, Blanche P. Alter, Anandani Nellan, Christopher Gamper, Kip R. Hartman, Sharon A. Savage, Sara Bass, Joseph F. Boland, Laurie Burdett, Salma Chowdhury, Michael Cullen, Casey Dagnall, Herbert Higson, Amy Hutchinson, Kristine Jones, Sally Larson, Kerrie Lashley, Hyo‐Jung Lee, Wen Luo, Michael Malasky, Jason Mitchell, David A. Roberson, Aurélie Vogt, Mingyi Wang, Meredith Yeager, Xijun Zhang, Neil E. Caporaso, Stephen J. Chanock, Mark H. Greene, Lynn R. Goldin, Alisa M. Goldstein, Allan Hildesheim, Nan Hu, Maria Teresa Landi, Jennifer T. Loud, L. Phuong, Mary L. McMaster, Kari G. Rabe, Lindsay M. Morton, Melissa Rotunno, Douglas R. Stewart, Phil R. Taylor, Geoffrey S. Tobias, Margaret A. Tucker, Xiaohong R. Yang, Guoqin Yu,

Connexins and lens biology

Hoyeraal-Hreidarsson syndrome is a dyskeratosis congenita-related telomere biology disorder that presents in infancy with intrauterine growth retardation, immunodeficiency, and cerebellar hypoplasia in addition to the triad of nail dysplasia, skin pigmentation, and oral leukoplakia. Individuals with Hoyeraal-Hreidarsson syndrome often develop bone marrow failure in early childhood. Germline mutations in DKC1, TERT, TINF2, RTEL1, ACD, or PARN cause about 60% of individuals with Hoyeraal-Hreidarsson syndrome.We describe 14 years of follow-up of an individual with Hoyeraal-Hreidarsson syndrome who initially presented as an infant with intrauterine growth retardation, microcephaly, and central nervous system calcifications. He was diagnosed with Hoyeraal-Hreidarsson syndrome at age 6 years and had a complicated medical history including severe developmental delay, cerebellar hypoplasia, esophageal and urethral stenosis, hip avascular necrosis, immunodeficiency, and bone marrow failure evolving to myelodysplastic syndrome requiring hematopoietic cell transplantation at age 14 years. He had progressive skin pigmentation, oral leukoplakia, and nail dysplasia leading to anonychia. Whole exome sequencing identified novel biallelic variants in PARN.This patient illustrates that the constellation of intrauterine growth retardation, central nervous system calcifications, and cerebellar hypoplasia, esophageal or urethral stenosis, and cytopenias, in the absence of congenital infection, may be due to Hoyeraal-Hreidarsson syndrome. Early diagnosis of Hoyeraal-Hreidarsson syndrome is important to optimize medical management and provide genetic counseling.