Hipotonik İnfant
References
Nimmo GAM, Cohn RD. The Floppy Infant. In: Swaiman KF, Ashwal S, Ferriero DM, Schor NF, Finkel RS, Gropman AL, Pearl PL, Shevel MI (eds.) Swaiman’s Pediatric Neurology. 6th ed. China: Elsevier; 2018. p.1051-1056.
Fenichel GM. Klinik Çocuk Nörolojisi. (Vildan BAYTOK, Çev. Ed.). Adana: Adana Nobel Kitabevi;2010.
Swaiman KF, Phillips J. Muscular Tone and Gait Disturbances. In: Swaiman KF, Ashwal S, Ferriero DM, Schor NF, Finkel RS, Gropman AL, Pearl PL, Shevel MI (eds.) Swaiman’s Pediatric Neurology. 6th ed. China: Elsevier; 2018. p.27-32.
Bodensteiner JB. The evaluation of the hypotonic infant. Semin Pediatr Neurol. 2008;15(1):10-20. doi:10.1016/j.spen.2008.01.003
Kumandaş S, Gümüş H. Hipotoni İnfant. In: Gökçay E, Sönmez M, Topaloğlu H, Tekgül H, Gürer Y (eds.). Çocuk Nörolojisi. 2nd ed. Ankara: Türkiye Çocuk Nöroloji Derneği; 2010. p.475-482.
Birdi K, Prasad AN, Prasad C, Chodirker B, Chudley AE. The floppy infant:retrospective analysis of clinical experience (1990-2000) in a tertiary care facility. J Child Neurol 2005;20:803-808. doi: 10.1177/08830738050200100401
Bayram E, Yiş U, Hız Kurul S. Hipotonik infant: Klinik ve etyolojik değerlendirme. DEÜ Tıp Fakültesi Dergisi 2012;26(3):219-228.
Paro-Panjan D, Neubauer D. Congenital hypotonia: is there an algorithm?. J Child Neurol. 2004;19(6):439-442. doi:10.1177/088307380401900608
Richer LP, Shevell MI, Miller SP. Diagnostic profile of neonatal hypotonia: an 11-year study. Pediatr Neurol. 2001;25(1):32-37. doi:10.1016/s0887-8994(01)00277-6
Kang PB, Mercuri E. Laboratory Assement of the Child with Suspected Neuromuscular Disorders. In: Swaiman KF, Ashwal S, Ferriero DM, Schor NF, Finkel RS, Gropman AL, Pearl PL, Shevel MI (eds.) Swaiman’s Pediatric Neurology. 6th ed. China: Elsevier; 2018. p.1038-1043.
Mercuri E, Finkel RS, Muntoni F, et al. Diagnosis and management of spinal muscular atrophy: Part 1: Recommendations for diagnosis, rehabilitation, orthopedic and nutritional care. Neuromuscul Disord. 2018;28(2):103-115. doi:10.1016/j.nmd.2017.11.005
Chen TH. New and Developing Therapies in Spinal Muscular Atrophy: From Genotype to Phenotype to Treatment and Where Do We Stand?. Int J Mol Sci. 2020;21(9):3297. Published 2020 May 7. doi:10.3390/ijms21093297
Halk Sağlığı GenelMüdürlüğü. Yenidoğan Metabolik ve Endokrin Hastalık Tarama Programı 2017 (28.08.2022 tarihinde https://hsgm.saglik.gov.tr/tr/cocukergen-tp-liste/yenidogan_tarama_programi.html adresinden ulaşılmıştır).
Mehta P, Küspert M, Bale T, et al. Novel mutation in CNTNAP1 results in congenital hypomyelinating neuropathy. Muscle Nerve. 2017;55(5):761-765. doi:10.1002/mus.25416
Plante-Bordeneuve V, Said G. Dejerine-Sottas disease and hereditary demyelinating polyneuropathy of infancy. Muscle Nerve. 2002;26(5):608-621. doi:10.1002/mus.10197
Altuame FD, Foskett G, Atwal PS, et al. The natural history of infantile neuroaxonal dystrophy. Orphanet J Rare Dis. 2020;15(1):109. Published 2020 May 1. doi:10.1186/s13023-020-01355-2
Kaler J, Hussain A, Patel S, Majhi S. Neuromuscular Junction Disorders and Floppy Infant Syndrome: A Comprehensive Review. Cureus. 2020;12(2):e6922. Published 2020 Feb 8. doi:10.7759/cureus.6922
Butterfield RJ. Congenital Muscular Dystrophy and Congenital Myopathy. Continuum (Minneap Minn). 2019;25(6):1640-1661. doi:10.1212/CON.0000000000000792
Fenichel GM. Klinik Çocuk Nörolojisi. (Vildan BAYTOK, Çev. Ed.). Adana: Adana Nobel Kitabevi;2010.
Swaiman KF, Phillips J. Muscular Tone and Gait Disturbances. In: Swaiman KF, Ashwal S, Ferriero DM, Schor NF, Finkel RS, Gropman AL, Pearl PL, Shevel MI (eds.) Swaiman’s Pediatric Neurology. 6th ed. China: Elsevier; 2018. p.27-32.
Bodensteiner JB. The evaluation of the hypotonic infant. Semin Pediatr Neurol. 2008;15(1):10-20. doi:10.1016/j.spen.2008.01.003
Kumandaş S, Gümüş H. Hipotoni İnfant. In: Gökçay E, Sönmez M, Topaloğlu H, Tekgül H, Gürer Y (eds.). Çocuk Nörolojisi. 2nd ed. Ankara: Türkiye Çocuk Nöroloji Derneği; 2010. p.475-482.
Birdi K, Prasad AN, Prasad C, Chodirker B, Chudley AE. The floppy infant:retrospective analysis of clinical experience (1990-2000) in a tertiary care facility. J Child Neurol 2005;20:803-808. doi: 10.1177/08830738050200100401
Bayram E, Yiş U, Hız Kurul S. Hipotonik infant: Klinik ve etyolojik değerlendirme. DEÜ Tıp Fakültesi Dergisi 2012;26(3):219-228.
Paro-Panjan D, Neubauer D. Congenital hypotonia: is there an algorithm?. J Child Neurol. 2004;19(6):439-442. doi:10.1177/088307380401900608
Richer LP, Shevell MI, Miller SP. Diagnostic profile of neonatal hypotonia: an 11-year study. Pediatr Neurol. 2001;25(1):32-37. doi:10.1016/s0887-8994(01)00277-6
Kang PB, Mercuri E. Laboratory Assement of the Child with Suspected Neuromuscular Disorders. In: Swaiman KF, Ashwal S, Ferriero DM, Schor NF, Finkel RS, Gropman AL, Pearl PL, Shevel MI (eds.) Swaiman’s Pediatric Neurology. 6th ed. China: Elsevier; 2018. p.1038-1043.
Mercuri E, Finkel RS, Muntoni F, et al. Diagnosis and management of spinal muscular atrophy: Part 1: Recommendations for diagnosis, rehabilitation, orthopedic and nutritional care. Neuromuscul Disord. 2018;28(2):103-115. doi:10.1016/j.nmd.2017.11.005
Chen TH. New and Developing Therapies in Spinal Muscular Atrophy: From Genotype to Phenotype to Treatment and Where Do We Stand?. Int J Mol Sci. 2020;21(9):3297. Published 2020 May 7. doi:10.3390/ijms21093297
Halk Sağlığı GenelMüdürlüğü. Yenidoğan Metabolik ve Endokrin Hastalık Tarama Programı 2017 (28.08.2022 tarihinde https://hsgm.saglik.gov.tr/tr/cocukergen-tp-liste/yenidogan_tarama_programi.html adresinden ulaşılmıştır).
Mehta P, Küspert M, Bale T, et al. Novel mutation in CNTNAP1 results in congenital hypomyelinating neuropathy. Muscle Nerve. 2017;55(5):761-765. doi:10.1002/mus.25416
Plante-Bordeneuve V, Said G. Dejerine-Sottas disease and hereditary demyelinating polyneuropathy of infancy. Muscle Nerve. 2002;26(5):608-621. doi:10.1002/mus.10197
Altuame FD, Foskett G, Atwal PS, et al. The natural history of infantile neuroaxonal dystrophy. Orphanet J Rare Dis. 2020;15(1):109. Published 2020 May 1. doi:10.1186/s13023-020-01355-2
Kaler J, Hussain A, Patel S, Majhi S. Neuromuscular Junction Disorders and Floppy Infant Syndrome: A Comprehensive Review. Cureus. 2020;12(2):e6922. Published 2020 Feb 8. doi:10.7759/cureus.6922
Butterfield RJ. Congenital Muscular Dystrophy and Congenital Myopathy. Continuum (Minneap Minn). 2019;25(6):1640-1661. doi:10.1212/CON.0000000000000792
Pages
9-22
Published
April 17, 2023
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Polat İ. Hipotonik İnfant. In: Alabaz D, editor. Güncel Çocuk Sağlığı ve Hastalıkları V [Internet]. Türkiye: Academician Publishing Book DOI Portal; 2023 [cited 2026 Jul. 15]. pp. 9-22. Available from: https://omp35.books.akademisyen.net/index.php/akya/catalog/book/2565/chapter/13174