Clinical and Experimental Pediatrics

Original Article

Jae un, June Huh, Il Soo Ha, Hae Il Cheong, Yong Choi

Clin Exp Pediatr. 1994;37(3):376-382. Published online March 15, 1994

The clinical data of 27 patients with hypophosphatemic rickets treated with phosphate and 1 α-hydroxyvitamin D were analysed retrospectively. The median age at diagnosis was 4 years, and the main clinical manifestations were bowleg and short stature. Among total 24 families, 5 families(21%) had X-linked dominant mode of inheritance, 1 family (4%) had autosomal dominant mode and 17 families (71%)...

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Hypophosphatemic Rickets.

Kyung Mo Kim, Seong Hoon Ha, Dong Kyu Jin, Kwang Wook Ko

Clin Exp Pediatr. 1990;33(4):437-447. Published online April 30, 1990

Seventeen patients who were diagnosed as primary hypophosphatemic rickets at Department of Pediatrics, Seoul National University Children’s Hospital were analyzed to assess its clinical aspect and effect of treatment, especially on height and growth velosity. The average age of onset was 2 years, and their chief complaints were bowleg and short stature. Sex ratio was l.l:l(male: female). Familial hypophoshatemic rickets was known as X-linked...

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Clinical Study of Hypophosphatemic Rickets.

Seok Min Choi, Duk Hi Kim, Chin Suck Suh

Clin Exp Pediatr. 1989;32(8):1057-1063. Published online August 31, 1989

Hypophosphatemic rickets is a disorder characterized by a normal or slightly reduced serum calcium level, a moderately reduced serum phosphorus level and elevated alkaline phosphatase activity. The usual mode of inheritance is X-linked dominant and postulated mechanism is a selective disorder of tubular reabsorption of phosphate, defective conversion of 21-hydroxyvitamin D3 to calcitriol and increased catabolism of calcitriol. In children with renal hypophosphatemic rickets, growth...

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