Current Significance of Rickets Disease

نویسنده

  • Hosein Basheeri-Boad Department of Parasitology, Shahid Beheshti University School of Medicine, Tehran, Iran.
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Hypophosphatemic Rickets and its Dental Significance

I read with interest Rabbani et al’s paper entitled “Dental problems in hypophosphatemic rickets, a cross sectional study” in the fourth issue of Iran J Pediatr 2012[1]. Clinical oral manifestations of hypophosphatemic rickets often include premature tooth exfoliation, hypoplastic enamel and dental infections. Apical rarefaction, rickety bone trabeculation and absent or abnormal lamina dura are...

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Hypophosphatemic Rickets and its Dental Significance

Although the premature tooth exfoliation (PTE) can be associated with some systemic diseases such as changes in immune system or connective tissue disorders, we didn’t find any report on this disorder and hypophosphatemic rickets. In bone metabolic disorders, there are a few reports on hypophosphatasia and PTE[1-3]. Although, some factors such as severe oral infection can predispose PTE in HR p...

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Blount's disease: a rickets mimicker.

To cite: Bhattacharjee R, Chakraborty PP, Roy A, et al. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2016215682 DESCRIPTION A 6-year-old Indian girl presented with progressive bowing of both legs for the last 4.5 years (figure 1). She was diagnosed as having rickets by her primary care physician and was treated with multiple courses of vitamin D, without effect...

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Rickets: not a disease of the past.

Rickets develops when growing bones fail to mineralize. In most cases, the diagnosis is established with a thorough history and physical examination and confirmed by laboratory evaluation. Nutritional rickets can be caused by inadequate intake of nutrients (vitamin D in particular); however, it is not uncommon in dark-skinned children who have limited sun exposure and in infants who are breastf...

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Wilson’s Disease Presenting as Resistant Rickets

Wilson's disease is most common disorder of cooper metabolism. It has varied clinical presentations. We report a 12 years old female child presenting with genu valgum progressed over 6 months. Careful examination, high index of suspicion and investigations confirmed Wilson's disease.

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عنوان ژورنال

دوره 8  شماره 3

صفحات  191- 199

تاریخ انتشار 1985-05

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