Journals / Gülhane Tıp Dergisi / 2002 / Cilt: 44 - Sayı: 4

A rare rickets case: Hypophosphatemic rickets

Nadir bir rikets olgusus: Hipofosfatemik rikets

Pages
450–452
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In this paper by introducing a hypophosphatemic rickets case, which fall into the group of rickets resistant to vitamin D, the importance of both the existence of a different type of rickets and early diagnosis have been stressed.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Rickets, though a metabolic disorder seen especially as a result of exogenous vitamin D deficiency, is a childhood disease whose frequency of occurrence has gradually diminished thanks to the improvement in the standarts of both health and nutrition.
📊
Key Findings & Data:However, some different types of this disease that can occur with various etiopathogenic mechanisms are relatively rarely seen.
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Conclusion & Impact:In this paper by introducing a hypophosphatemic rickets case, which fall into the group of rickets resistant to vitamin D, the importance of both the existence of a different type of rickets and early diagnosis have been stressed.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Hipofosfatemi · Vitamin D · Raşitizm

Abstract

Rickets, though a metabolic disorder seen especially as a result of exogenous vitamin D deficiency, is a childhood disease whose frequency of occurrence has gradually diminished thanks to the improvement in the standarts of both health and nutrition. However, some different types of this disease that can occur with various etiopathogenic mechanisms are relatively rarely seen. In this paper by introducing a hypophosphatemic rickets case, which fall into the group of rickets resistant to vitamin D, the importance of both the existence of a different type of rickets and early diagnosis have been stressed.

Özet

Rikets, özellikle ekzojen D vitamini eksikliği sonucu görülen metabolik bir bozukluk olup günümüzde beslenme ve sağlık koşullarının düzelmesi ile görülme sıklığı giderek azalmış bir çocukluk çağı hastalığıdır. Hastalığın değişik etyopatogenetik mekanizmalarla gelişebilen farklı tipleri daha nadir olarak görülmektedir. Burada D vitaminine dirençli rikets kapsamında yer alan bir hipofosfatemik rikets olgusu sunularak farklı bir rikets tipinin ve erken tanının önemi vurgulanmıştır.

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Cite This Article

GÖK, F., KALMAN, S. (2002). A rare rickets case: Hypophosphatemic rickets. Gülhane Tıp Dergisi, Cilt: 44 - Sayı: 4, 450–452. https://ajindex.com/articles/225813

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References (7)

  1. Chesney, W.R.: Bone Disease. Nelson, W.E., Behrman, R.E., Kliegran, R.M., An/in, A.M.: in Nelson Textbook of Pediatrics. 15 eds., Pennsylvania, WB Saunders Co., 1996, p. 1984- 1990
  2. Hochberg, Z.: Rickets: it's not just vitamin D defi¬ ciency. Curr Opin Endocrinol & Diabetes 8:23- 28, 2001
  3. Dursun, A., Coşkun, T: Hipofosfatemik riketsde uzun süreli izlem. Eds: Özalp, I., Tuncer, M. Katkı Pediatri Dergisi, Ankara, 20(4), 536-550, 1999
  4. Joiner, T.A., Foster, C, Shope, T: The many faces of vitamin D defıcinency rickets. Pediatr Rev 21(9): 296-302, 2001
  5. Holm, I.A., Nelson, A.E., Robinson, B.G., et ai: Mutational analysis and genotype-phenotype correlation of the PHEX gene in X-linked hypophosphatemic rickets. J Clin Endocrinol Metab 86: 3889-99, 2001. 6. van den Heuvel, L, Koul, K.O., Knots, E.: Autosomal recessive hypophosphatemic rickets with hypercalciuria is not caused by mutations in the type II renal sodium/phosphate cotransporter gene. Nephrol Dial Transplant 16: 48-51, 2001
  6. Deeb, A.A., Bruce, S.N., Morris, A.A., et ai: Infantile hypophosphatasia: disappinting results of treatment. Ada Pediatr 89 (6): 730-3, 2000
  7. Tieder, M., Arie, R., Bab, I.: A new kindred with hereditary hypophosphatemic rickets with hypercalciuria: Implications for correct diagnosis and treatment. Nephron 62: 178-181,1992.