TY - JOUR AU - Asirvatham, A. R. AU - Mahadevan, S. AU - Balachandran, K. AU - Balasubramaniam, S. K. PY - 2018 DA - 2018// TI - Van Wyk Grumbach syndrome: a case series and review of literature JO - Int J Sci Res VL - 7 ID - Asirvatham2018 ER - TY - JOUR AU - Wyk, J. J. AU - Grumbach, M. M. PY - 1960 DA - 1960// TI - Syndrome of precocious menstruation and galactorrhoea in juvenile hypothyroidism: an example of hormonal overlap in pituitary feedback JO - J Pediatr VL - 57 UR - https://doi.org/10.1016/S0022-3476(60)80250-8 DO - 10.1016/S0022-3476(60)80250-8 ID - Wyk1960 ER - TY - JOUR AU - Zhang, S. AU - Yang, J. AU - Zheng, R. AU - Jiang, L. AU - Wei, Y. AU - Liu, G. PY - 2017 DA - 2017// TI - Van Wyk-Grumbach syndrome in a male pediatric patient: a rare case report and literature review JO - Exp Ther Med VL - 13 UR - https://doi.org/10.3892/etm.2017.4086 DO - 10.3892/etm.2017.4086 ID - Zhang2017 ER - TY - JOUR AU - Indumathi, C. K. AU - Bantwal, G. AU - Patil, M. PY - 2007 DA - 2007// TI - Primary hypothyroidism with precious puberty and bilateral cystic ovaries JO - Indian J Pediatr VL - 74 UR - https://doi.org/10.1007/s12098-007-0140-9 DO - 10.1007/s12098-007-0140-9 ID - Indumathi2007 ER - TY - JOUR AU - Baranowski, E. AU - Högler, W. PY - 2012 DA - 2012// TI - An unusual presentation of acquired hypothyroidism: the Van Wyk-Grumbach syndrome JO - Eur J Endocrinol VL - 166 UR - https://doi.org/10.1530/EJE-11-0494 DO - 10.1530/EJE-11-0494 ID - Baranowski2012 ER - TY - JOUR AU - Asami, T. AU - Kikuchi, T. AU - Kamimura, S. AU - Kinoshita, S. AU - Uchiyama, M. PY - 2001 DA - 2001// TI - Precocious puberty in a girl with congenital hypothyroidism receiving continuous L-thyroxine-replacement therapy JO - Pediatr Int VL - 43 UR - https://doi.org/10.1046/j.1442-200x.2001.01318.x DO - 10.1046/j.1442-200x.2001.01318.x ID - Asami2001 ER - TY - JOUR AU - Razi, S. M. AU - Gupta, A. K. AU - Gupta, D. C. AU - Gutch, M. AU - Gupta, K. K. AU - Usman, S. I. PY - 2017 DA - 2017// TI - Van Wyk-Grumbach syndrome with Kocher-Debré-Sémélaigne srndrome: case report of a rare association JO - Eur Thyroid J VL - 6 UR - https://doi.org/10.1159/000448993 DO - 10.1159/000448993 ID - Razi2017 ER - TY - JOUR AU - Marzuilla, P. AU - Grandone, A. AU - Perrotta AU - Ruggiero, L. AU - Capristo, C. AU - Luongo, C. PY - 2016 DA - 2016// TI - Very early onset of autoimmune thyroiditis in a toddler with severe hypothyroidism presentation: a case report JO - Ital J Pediatr VL - 42 UR - https://doi.org/10.1186/s13052-016-0270-7 DO - 10.1186/s13052-016-0270-7 ID - Marzuilla2016 ER - TY - JOUR AU - Anasti, J. N. AU - Flack, M. R. AU - Froehlich, J. AU - Nelson, L. M. AU - Nisula, B. C. PY - 1995 DA - 1995// TI - A potential novel mechanism for precocious puberty in juvenile hypothyroidism JO - J Clin Endocrinol Metab VL - 80 ID - Anasti1995 ER - TY - JOUR AU - Sharma, D. AU - Dayal, D. AU - Gupta, A. AU - Saxena, A. PY - 2011 DA - 2011// TI - Premature menarche associated with primary hypothyroidism in a 5.5 year old girl JO - Case Rep Endocrinol VL - 2011 ID - Sharma2011 ER - TY - JOUR AU - Wormsbecker, A. AU - Clarson, C. PY - 2010 DA - 2010// TI - Acquired primary hypothyroidism: vaginal bleeding in a quiet child JO - Can Med Assoc J VL - 182960 UR - https://doi.org/10.1503/cmaj.090883 DO - 10.1503/cmaj.090883 ID - Wormsbecker2010 ER - TY - STD TI - Cetinkaya S, Sagsak E, Erdeve S, Aycan Z, Keskin M. Premature menarche associated with Hashimoto thyroiditis at 2 years 9 months: case report. Thyroid Disorders Ther. 2014;3:159. ID - ref12 ER - TY - JOUR AU - Thackray, V. G. AU - Mellon, P. L. AU - Coss, D. PY - 2010 DA - 2010// TI - Hormones in synergy: regulation of the pituitary gonadotropin genes JO - Mol Cell Endocrinol VL - 314 UR - https://doi.org/10.1016/j.mce.2009.09.003 DO - 10.1016/j.mce.2009.09.003 ID - Thackray2010 ER - TY - JOUR AU - Durbin, K. L. AU - Diaz-Montes, T. AU - Loveless, M. B. PY - 2011 DA - 2011// TI - Van Wyk Grumbach Syndrome: an unusual case and review of literature JO - J Pediatr Adolesc Gynecol VL - 24 UR - https://doi.org/10.1016/j.jpag.2010.08.003 DO - 10.1016/j.jpag.2010.08.003 ID - Durbin2011 ER - TY - JOUR AU - Passeri, E. AU - Tufano, A. AU - Locatelli, M. AU - Lania, A. G. AU - Ambrosi, B. AU - Corbetta, S. PY - 2011 DA - 2011// TI - Large pituitary hyperplasia in severe primary hypothyroidism JO - J Clin Endocrinol Metab VL - 96 UR - https://doi.org/10.1210/jc.2010-2011 DO - 10.1210/jc.2010-2011 ID - Passeri2011 ER - TY - JOUR AU - Chu, J. Y. AU - Monteleone, J. A. AU - Peden, V. H. AU - Graviss, E. R. AU - Vernava, B. S. PY - 1981 DA - 1981// TI - Anaemia in children and adolescents with hypothyroidism JO - Clin Pediatr VL - 20 UR - https://doi.org/10.1177/000992288102001102 DO - 10.1177/000992288102001102 ID - Chu1981 ER - TY - JOUR AU - Purkait, R. AU - Prasad, A. AU - Bhadra, R. AU - Basu, A. PY - 2013 DA - 2013// TI - Massive pericardial effusion as the only manifestation of primary hypothyroidism JO - J Cardiovasc Dis Res VL - 4 ID - Purkait2013 ER - TY - JOUR AU - Deng, H. AU - Tan, T. PY - 2015 DA - 2015// TI - Advances in the molecular genetics of non-syndromic syndactyly JO - Curr Genomics VL - 16 UR - https://doi.org/10.2174/1389202916666150317233103 DO - 10.2174/1389202916666150317233103 ID - Deng2015 ER - TY - JOUR AU - Kariminejad, A. AU - Stollfuβ, B. AU - Li, Y. AU - Bögershausen, N. AU - Boss, K. AU - Hennekam, R. C. PY - 2013 DA - 2013// TI - Severe Cenani-Lenz syndrome caused by loss of LRP4 function JO - Am J Med Genet VL - 161A UR - https://doi.org/10.1002/ajmg.a.35920 DO - 10.1002/ajmg.a.35920 ID - Kariminejad2013 ER - TY - JOUR AU - Hettiaracchchi, D. AU - Bonnard, C. AU - Jayawardana, S. M. A. AU - Jin Ng, A. Y. AU - Tohari, S. AU - Venkates, B. PY - 2018 DA - 2018// TI - Cenani-Lenz Syndactyly syndrome - a case report of a family with isolated syndactyly JO - BMC Med Genet VL - 19 UR - https://doi.org/10.1186/s12881-018-0646-1 DO - 10.1186/s12881-018-0646-1 ID - Hettiaracchchi2018 ER - TY - STD TI - JJarbhoua H, Hamamya H, Al-Hadidyb A, Ajlounia K. Cenani–Lenz syndactyly with facial dysmorphism, hypothyroidism, and renal hypoplasia: a case report. Clin Dysmorphol. 2008;17:269-70. ID - ref21 ER - TY - JOUR AU - Smets, G. AU - Vankan, Y. AU - Demeyere, A. PY - 2016 DA - 2016// TI - A female newborn infant with FATCO syndrome variant (fibular hypoplasia, tibial campomelia, oligosyndactyly) – a case report JO - J Belgian Soc Radiol VL - 100 UR - https://doi.org/10.5334/jbr-btr.929 DO - 10.5334/jbr-btr.929 ID - Smets2016 ER - TY - JOUR AU - Wilcow, W. AU - Coulter, C. P. AU - Schmitz, M. L. PY - 2015 DA - 2015// TI - Congenital limb deficiency disorders JO - Clin Perinatol VL - 42 UR - https://doi.org/10.1016/j.clp.2015.02.004 DO - 10.1016/j.clp.2015.02.004 ID - Wilcow2015 ER - TY - JOUR AU - Stevens, P. AU - Arms, D. PY - 2000 DA - 2000// TI - Postaxial hypoplasia of the lower extremity JO - J Pediatr Orthop B VL - 20 ID - Stevens2000 ER - TY - JOUR AU - Hulinsky, R. AU - Byrne, J. B. L. AU - Lowichik, A. AU - Viskochil, D. H. PY - 2005 DA - 2005// TI - Fetus with interstitial del (5)(p13.1p14.2) diagnosed postnatally with Cornelia de Lange syndrome JO - Am J Med Genet VL - 137A UR - https://doi.org/10.1002/ajmg.a.30856 DO - 10.1002/ajmg.a.30856 ID - Hulinsky2005 ER - TY - JOUR AU - Bosse, K. AU - Betz, R. C. AU - Lee, Y. A. AU - Wienker, T. F. AU - Reis, A. AU - Kleen, H. PY - 2000 DA - 2000// TI - Localization of a gene for syndactyly type a to chromosome 2q34-q36 JO - Am J Hum Genet VL - 67 UR - https://doi.org/10.1086/303028 DO - 10.1086/303028 ID - Bosse2000 ER -