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THE MUSCULOSKELETAL SIDE EFFECTS OF ORAL ISOTRETINOIN: A NARRATIVE REVIEW

Year 2025, Volume: 6 Issue: 3, 255 - 261, 25.11.2025

Abstract

Introduction: This narrative review aims to summarize the current literature on the musculoskeletal adverse effects of oral isotretinoin, discuss potential mechanisms and clinical implications, and highlight key considerations for clinicians in patient monitoring.

Method: Publications between January 1983 and August 2025 were reviewed through PubMed, Google Scholar, and ScienceDirect. The keywords “isotretinoin”, “retinoids”, “musculoskeletal system,” “sacroiliitis,” “spondylarthropathies,” “arthritis,” “hyperostosis,” “osteoporosis,” “hypercalcemia,” “myalgia,” “creatine kinase” and “rhabdomyolysis” were used. Only English-language publications were included. No formal methodological quality scale was applied; instead, study relevance, sample quality, and clinical contribution were considered. Systematic reviews, clinical studies, case series, and case reports were included. The findings were summarized in a narrative manner and evaluated in terms of clinical practice.

Results: Musculoskeletal adverse effects of isotretinoin include axial like symptoms (e.g., inflammatory back pain, sacroiliitis, enthesitis), peripheral arthritis, hyperostosis, premature epiphyseal closure, osteoporosis, hypercalcemia, myalgia, and elevated creatine kinase levels. Back pain, arthralgia, and myalgia are the most common side effects, typically emerging within the first three months of treatment. Sacroiliitis is usually acute, HLA-B27-negative, and resolves after drug discontinuation. Bone effects are primarily observed with prolonged, high cumulative doses, whereas vitamin D metabolism may be affected even in short courses. Muscle involvement is generally mild but may rarely lead to rhabdomyolysis with intensive exercise.

Conclusion: Musculoskeletal side effects of isotretinoin are generally mild and reversible but may mimic spondyloarthropathies or other rheumatologic disorders. Awareness, baseline risk assessment (including vitamin D status), and early recognition are essential to avoid misdiagnosis and unnecessary interventions. Collaboration between dermatology and musculoskeletal specialists is recommended for optimal management.

Ethical Statement

Ethical approval: This study did not involve human or animal subjects; therefore, obtaining approval from an ethics committee was deemed unnecessary.

Supporting Institution

none

References

  • Zaenglein AL, Davis SA, McClain RW, Eichenfield LF, Feldman SR. AAD guidelines update: management of acne vulgaris. J Am Acad Dermatol. 2024;90(1):1-12. doi:10.1016/j.jaad.2023.10.001.
  • McLane J. Analysis of common side effects of isotretinoin. J Am Acad Dermatol. 2001;45(5 Suppl):S188-94.
  • Almutairi RR, Almutairi AG, Alhallafi AF, et al. Isotretinoin musculoskeletal side effects: a systematic review. Dermatol Rep. 2024;16(4):9845. doi:10.4081/dr.2024.9845.
  • Karaosmanoğlu N, Mülkoğlu C. Analysis of musculoskeletal side effects of oral isotretinoin treatment: a cross-sectional study. BMC Musculoskelet Disord. 2020;21:631.
  • Kapała J, Lewandowska J, Placek W, Owczarczyk-Saczonek A. Adverse events in isotretinoin therapy: a single-arm meta-analysis. Int J Environ Res Public Health. 2022 May 26;19(11):6463. doi: 10.3390/ijerph19116463.
  • Alkan S, Kayıran N, Yılmaz S, Can B, Erdem T, Babaoğlu S, et al. Musculoskeletal side effects of isotretinoin. J Rheumatol. 2015;42(11):2098-103
  • Baykal-Selçuk L, Aksu Arıca D, Yaylı S, Özçelik S. Musculoskeletal findings during isotretinoin therapy. Cutan Ocul Toxicol. 2017;36(2):176-9.
  • Elnady B. New onset of axial spondyloarthritis during isotretinoin therapy. Clin Rheumatol. 2020;39:1829-38.
  • Zhao S, Sun W, Peng L, et al. Clinical features, treatment, and outcome of isotretinoin-associated sacroiliitis. Arthritis Res Ther. 2025;27:115. doi:10.1186/s13075-025-03582-z.
  • Dinçer Ü, Çakar E, Kıralp MZ, Dursun H. Isotretinoin may cause sacroiliitis: three cases. Turk J Rheumatol. 2008;23:157-9.
  • Agak GW, Qin M. Propionibacterium acnes induces an interleukin-17 response in acne vulgaris that is regulated by vitamin A and vitamin D. J Invest Dermatol. 2014;134(2):366-73.
  • Eksioglu E. Sacroiliitis and polyneuropathy during isotretinoin treatment. Clin Exp Dermatol. 2008;33(2):122-4. doi:10.1111/j.1365-2230.2007.02532.x.
  • Acar EM, Şaş S, Koçak FA. Isotretinoin-associated arthritis: case report. Arch Rheumatol. 2022;37(2):223-9.
  • Bottomley WW, Cunliffe WJ. Acute Achilles tendonitis following oral isotretinoin therapy for acne vulgaris. Clin Exp Dermatol. 1992;17(4):250-1. doi:10.1111/j.1365-2230.1992.tb02159.x.
  • Matsuoka LY, Wortsman J, Pepper JJ. Acute arthritis during isotretinoin treatment for acne. Arch Intern Med. 1984;144(9):1870-1.
  • Tasdelen OY, Yurdakul FG, Duran S, Bodur H. Isotretinoin-induced arthritis mimicking both rheumatoid arthritis and axial spondyloarthritis. Int J Rheum Dis. 2015;18(4):466-9.
  • Parada-Artunduaga MD, Cáceres-Bedoya JJ, Rojas-Villarraga A. Isotretinoin-induced arthritis: a rare but feasible diagnosis. Rev Colomb Reumatol (Engl Ed). 2022;29(4):314-8.
  • Luthi F, Eggel Y, Theumann N. Isotretinoin-related arthritis: case report. Joint Bone Spine. 2012;79(3):314-6.
  • Duvalyan A, Cha A, Goodarzian F, Arkader A, Villablanca JG, Marachelian A. Premature epiphyseal growth plate arrest after isotretinoin therapy for high-risk neuroblastoma: a case series and review of the literature. Pediatr Blood Cancer. 2020;67(8):e28236. doi:10.1002/pbc.28236.
  • Park WK, Choi HS, Chung CY, Park MS, Sung KH. Genu varum deformity due to premature epiphyseal closure after treatment with isotretinoin for neuroblastoma: a case report. J Orthop Surg (Hong Kong). 2020;28(2):2309499020924483. doi: 10.1177/2309499020924483
  • Alazawi S, Hendriksz T. Analysis of the effects of isotretinoin on the premature epiphyseal closure in pediatric populations: a literature review. J Osteopath Med. 2021 Oct 11;122(1):45-53. doi: 10.1515/jom-2021-0108.
  • Pittsley RA, Yoder FW. Retinoid hyperostosis: skeletal toxicity associated with long-term isotretinoin. N Engl J Med. 1983;308(17):1012-4.
  • Kilcoyne RF, Cope R, Cunningham W, et al. Minimal spinal hyperostosis with low-dose isotretinoin therapy. Invest Radiol. 1986;21(1):41-4.
  • Chamot AM, Benhamou CL, Kahn MF, Beraneck L, Kaplan G, Prost A. Le syndrome acné pustulose hyperostose ostéite (SAPHO). Rev Rhum Mal Osteoartic. 1987;54(3):187-96.
  • Ibáñez Barceló M, Estremera Rodrigo A, Ros Vilamajó I, Juan Mas A. Diffuse idiopathic skeletal hyperostosis in a young woman treated with isotretinoin. Reumatol Clin (Engl Ed). 2020;S1699-258X(20)30229-1.
  • Melhus H, Michaëlsson K, Kindmark A, et al. Excessive dietary intake of vitamin A is associated with reduced bone mineral density and increased risk for hip fracture. Ann Intern Med. 1998 Nov 15;129(10):770-8. doi: 10.7326/0003-4819-129-10-199811150-00003.
  • Rejnmark L, Vestergaard P, Charles P, Hermann AP, Brot C, Eiken P, Mosekilde L. No effect of vitamin A intake on bone mineral density and fracture risk in perimenopausal women. Osteoporos Int. 2004 Nov;15(11):872-80. doi: 10.1007/s00198-004-1618-1.
  • Valentic JP, Elias AN, Weinstein GD. Hypercalcemia associated with oral isotretinoin in the treatment of severe acne. JAMA. 1983 Oct 14;250(14):1899-900.
  • Belden TL, Ragucci DP. Hypercalcemia induced by 13-cis-retinoic acid in a patient with neuroblastoma. Pharmacotherapy. 2002 May;22(5):645-8. doi: 10.1592/phco.22.8.645.33207.
  • Cross SF, Dalla Pozza L, Munns CF. Hypercalcemia and osteoblastic lesions induced by 13-cis-retinoic acid mimicking relapsed neuroblastoma. Pediatr Blood Cancer. 2009 Oct;53(4):666-8. doi: 10.1002/pbc.22052.
  • Hoemberg M, Schwenzfeur R, Berthold F, Simon T, Hero B. Hypercalcemia is a frequent side effect of 13-cis-retinoic acid treatment in patients with high-risk neuroblastoma. Pediatr Blood Cancer. 2022;69(2):e29374. doi:10.1002/pbc.29374.
  • Ertugrul DT, Karadag AS, Tutal E, Akin KO. Therapeutic hotline. Does isotretinoin have effect on vitamin D physiology and bone metabolism in acne patients? Dermatol Ther. 2011 Mar-Apr;24(2):291-5. doi: 10.1111/j.1529-8019.2011.01406.x.
  • Johansson S, Melhus H. Vitamin A antagonizes calcium response to vitamin D in man. J Bone Miner Res. 2001 Oct;16(10):1899-905. doi: 10.1359/jbmr.2001.16.10.1899.
  • DiGiovanna JJ, Langman CB, Tschen EH, et al. Effect of a single course of isotretinoin therapy on bone mineral density in adolescent patients with severe, recalcitrant, nodular acne. J Am Acad Dermatol. 2004 Nov;51(5):709-17. doi: 10.1016/j.jaad.2004.04.032.
  • Cleary MA, Sadowski KA, Lee SY, Miller GL, Nichols AW. Exertional rhabdomyolysis in an adolescent athlete during preseason conditioning: a perfect storm. J Strength Cond Res. 2011 Dec;25(12):3506-13. doi: 10.1519/JSC.0b013e318216302f.
  • Marson JW, Baldwin HE. The creatine kinase conundrum: a reappraisal of the association of isotretinoin, creatine kinase, and rhabdomyolysis. Int J Dermatol. 2020 Mar;59(3):279-83. doi: 10.1111/ijd.14758.
  • Landau M, Mesterman R, Ophir J, et al. Clinical significance of markedly elevated serum creatine kinase levels in patients with acne on isotretinoin. Acta Derm Venereol. 2001 Oct-Nov;81(5):350-2. doi: 10.1080/000155501317140070.
  • Sargin B, Manzo C. Oral isotretinoin and sacroiliitis: causal link or coincidence? Discussion points emerging from a case-based review. Rheumatology. 2022;60(5):357–360. doi:10.5114/reum.2022.120761.
  • Karadağ ŞG, Sönmez HE, Tanatar A, Çakan M, Aktay Ayaz N. Isotretinoin-induced sacroiliitis: Case series of four patients and a systematic review of the literature. Pediatr Dermatol. 2020 Jan;37(1):171-175. doi: 10.1111/pde.14035.

ORAL İZOTRETİNOİNİN KAS-İSKELET SİSTEMİ YAN ETKİLERİ: ANLATISAL BİR DERLEME

Year 2025, Volume: 6 Issue: 3, 255 - 261, 25.11.2025

Abstract

Giriş: Bu anlatısal derlemenin amacı, oral izotretinoinin kas-iskelet sistemi üzerindeki advers etkilerine ilişkin güncel literatürü özetlemek, olası mekanizmaları ve klinik yansımaları tartışmak ve klinisyenler için izlemde dikkat edilmesi gereken temel noktaları vurgulamaktır

Yöntem: Ocak 1983–Ağustos 2025 arasında yayımlanmış literatür PubMed, Google Scholar ve ScienceDirect veri tabanlarında taranmıştır. Aramalarda “isotretinoin,” “retinoids,” “musculoskeletal system,” “sacroiliitis,” “spondylarthropathies,” “arthritis,” “hyperostosis,” “osteoporosis,” “hypercalcemia,” “myalgia,” “creatine kinase” ve “rhabdomyolysis” anahtar kelimeleri kullanılmıştır. Tarama sürecinde yalnızca İngilizce yayımlanmış makaleler değerlendirmeye alınmıştır. Çalışmaların metodolojik kalitesini değerlendirmek için resmi bir ölçek kullanılmamış; bunun yerine çalışmanın konuya uygunluğu, örneklem kalitesi ve klinik katkısı dikkate alınmıştır. Sistematik derlemeler, klinik çalışmalar, olgu serileri ve olgu sunumları dahil edilmiştir. Bulgular önceden belirlenen alt başlıklar altında anlatımsal biçimde sentezlenmiştir.

Bulgular: İzotretinoinin kas-iskelet sistemi üzerindeki yan etkileri: aksiyel spondiloartrit benzeri bulgular (inflamatuvar bel ağrısı, sakroiliit, entezit), periferik artrit, hiperostoz, erken epifiz kapanması, osteoporoz, hiperkalsemi, miyalji ve kreatin kinaz yüksekliği şeklinde ortaya çıkmaktadır. Bel ağrısı, artralji ve miyalji en sık görülen yan etkilerdir ve genellikle tedavinin ilk üç ayında ortaya çıkar. Sakroiliit olguları çoğunlukla akut, HLA-B27 negatif olup ilaç kesilmesiyle düzelir. Kemik etkileri genellikle uzun süreli, yüksek kümülatif dozlarla ilişkilidir; kısa süreli tedavilerde ise D vitamini metabolizması etkilenebilmektedir. Kas tutulumu çoğunlukla hafif seyirli olmakla birlikte yoğun egzersizle nadiren rabdomiyolize yol açabilir.

Sonuç: İzotretinoinin kas-iskelet sistemi üzerindeki yan etkileri genellikle hafif ve geri dönüşümlüdür; ancak spondiloartrit veya diğer romatolojik hastalıkları taklit edebilir. Yan etkilerin farkında olunması, D vitamini durumu dahil olmak üzere başlangıç risk değerlendirmesinin yapılması ve erken tanı, yanlış tanı ve gereksiz girişimlerin önlenmesi açısından kritik önemdedir. Dermatoloji ile kas-iskelet sistemi uzmanlarının iş birliği, hasta yönetimini optimize eder.
Anahtar kelimeler: izotretinoin; kas-iskelet sistemi; sakroiliit; spondiloartrit; hiperostoz; rabdomiyoliz.

Ethical Statement

Etik onay: Bu çalışma insan veya hayvan deneklerini içermedi; bu nedenle, bir etik komitesinden onay almak gereksiz kabul edildi.

Supporting Institution

yok

References

  • Zaenglein AL, Davis SA, McClain RW, Eichenfield LF, Feldman SR. AAD guidelines update: management of acne vulgaris. J Am Acad Dermatol. 2024;90(1):1-12. doi:10.1016/j.jaad.2023.10.001.
  • McLane J. Analysis of common side effects of isotretinoin. J Am Acad Dermatol. 2001;45(5 Suppl):S188-94.
  • Almutairi RR, Almutairi AG, Alhallafi AF, et al. Isotretinoin musculoskeletal side effects: a systematic review. Dermatol Rep. 2024;16(4):9845. doi:10.4081/dr.2024.9845.
  • Karaosmanoğlu N, Mülkoğlu C. Analysis of musculoskeletal side effects of oral isotretinoin treatment: a cross-sectional study. BMC Musculoskelet Disord. 2020;21:631.
  • Kapała J, Lewandowska J, Placek W, Owczarczyk-Saczonek A. Adverse events in isotretinoin therapy: a single-arm meta-analysis. Int J Environ Res Public Health. 2022 May 26;19(11):6463. doi: 10.3390/ijerph19116463.
  • Alkan S, Kayıran N, Yılmaz S, Can B, Erdem T, Babaoğlu S, et al. Musculoskeletal side effects of isotretinoin. J Rheumatol. 2015;42(11):2098-103
  • Baykal-Selçuk L, Aksu Arıca D, Yaylı S, Özçelik S. Musculoskeletal findings during isotretinoin therapy. Cutan Ocul Toxicol. 2017;36(2):176-9.
  • Elnady B. New onset of axial spondyloarthritis during isotretinoin therapy. Clin Rheumatol. 2020;39:1829-38.
  • Zhao S, Sun W, Peng L, et al. Clinical features, treatment, and outcome of isotretinoin-associated sacroiliitis. Arthritis Res Ther. 2025;27:115. doi:10.1186/s13075-025-03582-z.
  • Dinçer Ü, Çakar E, Kıralp MZ, Dursun H. Isotretinoin may cause sacroiliitis: three cases. Turk J Rheumatol. 2008;23:157-9.
  • Agak GW, Qin M. Propionibacterium acnes induces an interleukin-17 response in acne vulgaris that is regulated by vitamin A and vitamin D. J Invest Dermatol. 2014;134(2):366-73.
  • Eksioglu E. Sacroiliitis and polyneuropathy during isotretinoin treatment. Clin Exp Dermatol. 2008;33(2):122-4. doi:10.1111/j.1365-2230.2007.02532.x.
  • Acar EM, Şaş S, Koçak FA. Isotretinoin-associated arthritis: case report. Arch Rheumatol. 2022;37(2):223-9.
  • Bottomley WW, Cunliffe WJ. Acute Achilles tendonitis following oral isotretinoin therapy for acne vulgaris. Clin Exp Dermatol. 1992;17(4):250-1. doi:10.1111/j.1365-2230.1992.tb02159.x.
  • Matsuoka LY, Wortsman J, Pepper JJ. Acute arthritis during isotretinoin treatment for acne. Arch Intern Med. 1984;144(9):1870-1.
  • Tasdelen OY, Yurdakul FG, Duran S, Bodur H. Isotretinoin-induced arthritis mimicking both rheumatoid arthritis and axial spondyloarthritis. Int J Rheum Dis. 2015;18(4):466-9.
  • Parada-Artunduaga MD, Cáceres-Bedoya JJ, Rojas-Villarraga A. Isotretinoin-induced arthritis: a rare but feasible diagnosis. Rev Colomb Reumatol (Engl Ed). 2022;29(4):314-8.
  • Luthi F, Eggel Y, Theumann N. Isotretinoin-related arthritis: case report. Joint Bone Spine. 2012;79(3):314-6.
  • Duvalyan A, Cha A, Goodarzian F, Arkader A, Villablanca JG, Marachelian A. Premature epiphyseal growth plate arrest after isotretinoin therapy for high-risk neuroblastoma: a case series and review of the literature. Pediatr Blood Cancer. 2020;67(8):e28236. doi:10.1002/pbc.28236.
  • Park WK, Choi HS, Chung CY, Park MS, Sung KH. Genu varum deformity due to premature epiphyseal closure after treatment with isotretinoin for neuroblastoma: a case report. J Orthop Surg (Hong Kong). 2020;28(2):2309499020924483. doi: 10.1177/2309499020924483
  • Alazawi S, Hendriksz T. Analysis of the effects of isotretinoin on the premature epiphyseal closure in pediatric populations: a literature review. J Osteopath Med. 2021 Oct 11;122(1):45-53. doi: 10.1515/jom-2021-0108.
  • Pittsley RA, Yoder FW. Retinoid hyperostosis: skeletal toxicity associated with long-term isotretinoin. N Engl J Med. 1983;308(17):1012-4.
  • Kilcoyne RF, Cope R, Cunningham W, et al. Minimal spinal hyperostosis with low-dose isotretinoin therapy. Invest Radiol. 1986;21(1):41-4.
  • Chamot AM, Benhamou CL, Kahn MF, Beraneck L, Kaplan G, Prost A. Le syndrome acné pustulose hyperostose ostéite (SAPHO). Rev Rhum Mal Osteoartic. 1987;54(3):187-96.
  • Ibáñez Barceló M, Estremera Rodrigo A, Ros Vilamajó I, Juan Mas A. Diffuse idiopathic skeletal hyperostosis in a young woman treated with isotretinoin. Reumatol Clin (Engl Ed). 2020;S1699-258X(20)30229-1.
  • Melhus H, Michaëlsson K, Kindmark A, et al. Excessive dietary intake of vitamin A is associated with reduced bone mineral density and increased risk for hip fracture. Ann Intern Med. 1998 Nov 15;129(10):770-8. doi: 10.7326/0003-4819-129-10-199811150-00003.
  • Rejnmark L, Vestergaard P, Charles P, Hermann AP, Brot C, Eiken P, Mosekilde L. No effect of vitamin A intake on bone mineral density and fracture risk in perimenopausal women. Osteoporos Int. 2004 Nov;15(11):872-80. doi: 10.1007/s00198-004-1618-1.
  • Valentic JP, Elias AN, Weinstein GD. Hypercalcemia associated with oral isotretinoin in the treatment of severe acne. JAMA. 1983 Oct 14;250(14):1899-900.
  • Belden TL, Ragucci DP. Hypercalcemia induced by 13-cis-retinoic acid in a patient with neuroblastoma. Pharmacotherapy. 2002 May;22(5):645-8. doi: 10.1592/phco.22.8.645.33207.
  • Cross SF, Dalla Pozza L, Munns CF. Hypercalcemia and osteoblastic lesions induced by 13-cis-retinoic acid mimicking relapsed neuroblastoma. Pediatr Blood Cancer. 2009 Oct;53(4):666-8. doi: 10.1002/pbc.22052.
  • Hoemberg M, Schwenzfeur R, Berthold F, Simon T, Hero B. Hypercalcemia is a frequent side effect of 13-cis-retinoic acid treatment in patients with high-risk neuroblastoma. Pediatr Blood Cancer. 2022;69(2):e29374. doi:10.1002/pbc.29374.
  • Ertugrul DT, Karadag AS, Tutal E, Akin KO. Therapeutic hotline. Does isotretinoin have effect on vitamin D physiology and bone metabolism in acne patients? Dermatol Ther. 2011 Mar-Apr;24(2):291-5. doi: 10.1111/j.1529-8019.2011.01406.x.
  • Johansson S, Melhus H. Vitamin A antagonizes calcium response to vitamin D in man. J Bone Miner Res. 2001 Oct;16(10):1899-905. doi: 10.1359/jbmr.2001.16.10.1899.
  • DiGiovanna JJ, Langman CB, Tschen EH, et al. Effect of a single course of isotretinoin therapy on bone mineral density in adolescent patients with severe, recalcitrant, nodular acne. J Am Acad Dermatol. 2004 Nov;51(5):709-17. doi: 10.1016/j.jaad.2004.04.032.
  • Cleary MA, Sadowski KA, Lee SY, Miller GL, Nichols AW. Exertional rhabdomyolysis in an adolescent athlete during preseason conditioning: a perfect storm. J Strength Cond Res. 2011 Dec;25(12):3506-13. doi: 10.1519/JSC.0b013e318216302f.
  • Marson JW, Baldwin HE. The creatine kinase conundrum: a reappraisal of the association of isotretinoin, creatine kinase, and rhabdomyolysis. Int J Dermatol. 2020 Mar;59(3):279-83. doi: 10.1111/ijd.14758.
  • Landau M, Mesterman R, Ophir J, et al. Clinical significance of markedly elevated serum creatine kinase levels in patients with acne on isotretinoin. Acta Derm Venereol. 2001 Oct-Nov;81(5):350-2. doi: 10.1080/000155501317140070.
  • Sargin B, Manzo C. Oral isotretinoin and sacroiliitis: causal link or coincidence? Discussion points emerging from a case-based review. Rheumatology. 2022;60(5):357–360. doi:10.5114/reum.2022.120761.
  • Karadağ ŞG, Sönmez HE, Tanatar A, Çakan M, Aktay Ayaz N. Isotretinoin-induced sacroiliitis: Case series of four patients and a systematic review of the literature. Pediatr Dermatol. 2020 Jan;37(1):171-175. doi: 10.1111/pde.14035.
There are 39 citations in total.

Details

Primary Language English
Subjects Rheumatology and Arthritis
Journal Section Review
Authors

İbrahim Uludoğan 0009-0004-2022-0665

Murat Birtane 0000-0003-0294-4155

Publication Date November 25, 2025
Submission Date September 22, 2025
Acceptance Date October 31, 2025
Published in Issue Year 2025 Volume: 6 Issue: 3

Cite

APA Uludoğan, İ., & Birtane, M. (2025). THE MUSCULOSKELETAL SIDE EFFECTS OF ORAL ISOTRETINOIN: A NARRATIVE REVIEW. Eskisehir Medical Journal, 6(3), 255-261.
AMA Uludoğan İ, Birtane M. THE MUSCULOSKELETAL SIDE EFFECTS OF ORAL ISOTRETINOIN: A NARRATIVE REVIEW. Eskisehir Med J. November 2025;6(3):255-261.
Chicago Uludoğan, İbrahim, and Murat Birtane. “THE MUSCULOSKELETAL SIDE EFFECTS OF ORAL ISOTRETINOIN: A NARRATIVE REVIEW”. Eskisehir Medical Journal 6, no. 3 (November 2025): 255-61.
EndNote Uludoğan İ, Birtane M (November 1, 2025) THE MUSCULOSKELETAL SIDE EFFECTS OF ORAL ISOTRETINOIN: A NARRATIVE REVIEW. Eskisehir Medical Journal 6 3 255–261.
IEEE İ. Uludoğan and M. Birtane, “THE MUSCULOSKELETAL SIDE EFFECTS OF ORAL ISOTRETINOIN: A NARRATIVE REVIEW”, Eskisehir Med J, vol. 6, no. 3, pp. 255–261, 2025.
ISNAD Uludoğan, İbrahim - Birtane, Murat. “THE MUSCULOSKELETAL SIDE EFFECTS OF ORAL ISOTRETINOIN: A NARRATIVE REVIEW”. Eskisehir Medical Journal 6/3 (November2025), 255-261.
JAMA Uludoğan İ, Birtane M. THE MUSCULOSKELETAL SIDE EFFECTS OF ORAL ISOTRETINOIN: A NARRATIVE REVIEW. Eskisehir Med J. 2025;6:255–261.
MLA Uludoğan, İbrahim and Murat Birtane. “THE MUSCULOSKELETAL SIDE EFFECTS OF ORAL ISOTRETINOIN: A NARRATIVE REVIEW”. Eskisehir Medical Journal, vol. 6, no. 3, 2025, pp. 255-61.
Vancouver Uludoğan İ, Birtane M. THE MUSCULOSKELETAL SIDE EFFECTS OF ORAL ISOTRETINOIN: A NARRATIVE REVIEW. Eskisehir Med J. 2025;6(3):255-61.