Literature DB >> 10798150

Hypophosphatemic rickets: easy to diagnose, difficult to treat.

R K Garg1, N Tandon.   

Abstract

Hypophosphatemic rickets (HR) has generated a lot of interest in recent times. There is need to recognize this disorder and differentiate it from the more common nutritional rickets because the therapy is different. It is also important to emphasize that a detailed clinical examination with pedigree analysis and easily available biochemical tests are adequate to establish the diagnosis in most cases. This report presents three families with hypophosphatemic rickets. Interestingly, many of these patients had a mixed picture of HR and nutritional rickets. Their important features are described with special emphasis on early initiation of treatment with oral phosphate and stringent monitoring of renal functions to prevent development of irreversible renal insufficiency.

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Year:  1999        PMID: 10798150     DOI: 10.1007/bf02723852

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   1.967


  10 in total

1.  A micromethod for the determination of serum calcium.

Authors:  F W FALES
Journal:  J Biol Chem       Date:  1953-10       Impact factor: 5.157

2.  A CONVENIENT METHOD FOR DETERMINING SERUM AND BILE PHOSPHATASE ACTIVITY.

Authors:  E J King; A R Armstrong
Journal:  Can Med Assoc J       Date:  1934-10       Impact factor: 8.262

Review 3.  New perspectives on the biology and treatment of X-linked hypophosphatemic rickets.

Authors:  T O Carpenter
Journal:  Pediatr Clin North Am       Date:  1997-04       Impact factor: 3.278

4.  X-linked dominant hypophosphatemia is closely linked to DNA markers DXS41 and DXS43 at Xp22.

Authors:  M Mächler; D Frey; A Gal; U Orth; T F Wienker; A Fanconi; W Schmid
Journal:  Hum Genet       Date:  1986-07       Impact factor: 4.132

Review 5.  Rickets and the pathogenesis of impaired tubular transport of phosphate and other solutes.

Authors:  C R Scriver
Journal:  Am J Med       Date:  1974-07       Impact factor: 4.965

6.  Crosstransplantation of kidneys in normal and Hyp mice. Evidence that the Hyp mouse phenotype is unrelated to an intrinsic renal defect.

Authors:  T Nesbitt; T M Coffman; R Griffiths; M K Drezner
Journal:  J Clin Invest       Date:  1992-05       Impact factor: 14.808

7.  Chromosomal localization of the human renal sodium phosphate transporter to chromosome 5: implications for X-linked hypophosphatemia.

Authors:  F K Ghishan; S Knobel; M Dasuki; M Butler; J Phillips
Journal:  Pediatr Res       Date:  1994-04       Impact factor: 3.756

8.  Nephrocalcinosis in X-linked hypophosphatemia: effect of treatment versus disease.

Authors:  A Taylor; N H Sherman; M E Norman
Journal:  Pediatr Nephrol       Date:  1995-04       Impact factor: 3.714

9.  Osteomalacia--fifty five patients seen in a teaching institution over a 4 year period.

Authors:  J T Mathew; M S Seshadri; K Thomas; H Krishnaswami; A M Cherian
Journal:  J Assoc Physicians India       Date:  1994-09

10.  Abnormal vitamin D metabolism in the X-linked hypophosphatemic mouse.

Authors:  R A Meyer; R W Gray; M H Meyer
Journal:  Endocrinology       Date:  1980-11       Impact factor: 4.736

  10 in total

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