The arthropathy of familial hypophosphataemic osteomalacia (FHO)

1984 ◽  
Vol 5 (4) ◽  
pp. 209
Author(s):  
D.W. James ◽  
T.C.B. Stamp
2020 ◽  
Vol 70 (3) ◽  
pp. 207-210 ◽  
Author(s):  
J Paul ◽  
K E Cherian ◽  
N Thomas ◽  
T V Paul

Abstract Chronic heavy metal exposure and the health hazards that ensue are important public-health problems. We highlight the occurrence of hypophosphataemic osteomalacia due to chronic cadmium exposure in the silver industry in India. Three silversmiths presented similarly with clinical, biochemical and radiological evidence of hypophosphataemic osteomalacia. Considering their occupation, their blood samples were screened for heavy metals and were found to have toxic levels of cadmium. They were initiated on neutral phosphate and calcitriol. On follow-up, they reported significant reduction in severity of symptoms. It is essential to maintain a high index of suspicion in diagnosing this condition. A thorough knowledge of the occupational background of patients, as well as ambient conditions at the workplace is of utmost importance in contemplating the possibility of such rare occurrences. Moreover, regulatory agencies and policy makers ought to survey the silver industry and ensure that the metals used are within permissible safe limits of exposure.


Rheumatology ◽  
2020 ◽  
Vol 59 (8) ◽  
pp. 2166-2168 ◽  
Author(s):  
Raj Amarnani ◽  
Simon Travis ◽  
Muhammad Kassim Javaid

Bone ◽  
1994 ◽  
Vol 15 (4) ◽  
pp. 452-452
Author(s):  
PSN Rowe ◽  
J Goulding ◽  
F Francis ◽  
M Econs ◽  
A Read ◽  
...  

BMJ ◽  
1976 ◽  
Vol 2 (6028) ◽  
pp. 142-144 ◽  
Author(s):  
J F Mahony ◽  
J M Hayes ◽  
J P Ingham ◽  
S Posen

1979 ◽  
Vol 97 (1) ◽  
pp. 33-37 ◽  
Author(s):  
K.Y. Ahmed ◽  
Z. Varghese ◽  
J.F. Moorhead ◽  
M.R. Wills

1985 ◽  
Vol 100 (1-2) ◽  
pp. 13-18 ◽  
Author(s):  
S. O'malley ◽  
R. T. Ramsden ◽  
A. Latif ◽  
R. Kane ◽  
M. Davies

Author(s):  
Yasmine Makhlouf ◽  
Soumaya Boussaid ◽  
Houda Ajlani ◽  
Samia Jemmali ◽  
Sonia Rekik ◽  
...  

Background: Neurofibromatosis type 1 (NF1), also known as von Recklinghausen disease, is a one of the more common hereditary autosomal disorders. However, osteomalacia in neurofibromatosis type 1 is very rare tumour-induced osteomalacia; fibroblast growth factor-23 is usually implicated. Patients and methods: We report the case of a patient with a history of von Recklinghausen neurofibromatosis who presented with hypophosphataemic osteomalacia. Results: The patient was treated with high-dose calcitriol and oral phosphate with clinical improvement. Conclusion: Even though it is a rare entity, we must consider the diagnosis of hypophosphataemic osteomalacia in patients with neurofibromatosis in order to deliver appropriate treatment.


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