Dillon, BronwynFeben, CandiceSegal, DavidDu Plessis, JohannesReynders, DavidWainwright, RosalindPoole, JanetKrause, Amanda2021-04-082021-04-082020-08Dillon B, Feben C, Segal D, et al. Endocrine profiling in patients with Fanconi anemia, homozygous for a FANCG founder mutation. Molecular Genetics and Genomic Medicine 2020;8:e1351. https://doi.org/10.1002/mgg3.1351.2324-9269 (online)10.1002/mgg3.1351http://hdl.handle.net/2263/79369BACKGROUND : Fanconi anemia (FA) is phenotypically diverse, hereditary condition associated with bone marrow failure, multiple physical abnormalities, and an increased susceptibility to the development of malignancies. Less recognized manifestations of FA include endocrine abnormalities. International discourse has highlighted that these abnormalities are widespread among children and adults with FA. To date there has been no systematic study that has evaluated the endocrine abnormalities in a cohort of patients with FA, homozygous for a founder mutation (c.637_643del (p.Tyr213Lysfs*6)) in FANCG. The objectives of the study were to evaluate endocrine gland function in patients with FA of a single FA genotype, and to determine the frequency and nature of endocrine abnormalities in this group. METHODS : Cross‐sectional, descriptive study of 24 South African patients of African ancestry with FA (homozygous for a FANCG founder mutation). Outcomes measured included growth, pubertal status, growth hormone axis screening, thyroid gland function, glucose and insulin metabolism and bone age (BA). RESULTS : Endocrine dysfunction was present in 70.8% (17 of 24), including abnormal insulin‐like growth factor 1 (IGF‐1)/insulin‐like growth factor‐binding protein 3 (IGFBP‐3) in 25.0% (6 of 24), insulin resistance in 41.7% (10 of 24), abnormal thyroid function in 16.7% (4 of 24) and short stature in 45.8% (11 of 24). No abnormalities of glucose metabolism were identified. Abnormal pubertal status was seen in three males (12.5%). Abnormal BAs were present in 34.8% (8 of 23). CONCLUSION : Endocrine abnormalities occur at a high frequency in patients with FA, homozygous for a FANCG founder mutation, similar to other FA cohorts. Our data are specific to FA patients with a single genotype, and therefore provide the first genotype‐phenotype information on endocrine abnormalities in South African patients, homozygous for a FANCG founder mutation. Recommendations regarding endocrine screening in this patient subgroup are made, including, but not limited to, baseline testing of thyroid function, fasted insulin and glucose, and IGF‐1 and IGFBP‐3.en© 2020 The Authors. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License.Endocrine abnormalitiesFANCGFounder mutationShort statureThyroid functionFanconi anemia (FA)South African patientsAfrican ancestryHealth sciences articles SDG-03SDG-03: Good health and well-beingHealth sciences articles SDG-09SDG-09: Industry, innovation and infrastructureHealth sciences articles SDG-10SDG-10: Reduced inequalitiesArticle