\s=b\ We describe four children with idiopathic juvenile osteoporosis. All patients were initially seen between the ages of 10 and 13 years and spontaneously recovered following puberty. We review 27 similar cases reported in the literature. Theories on the cause of idiopathic osteoporosis in children are critically discussed. It may be that milder forms remain undiagnosed because of the self-limited course and the pain being confused with a variety of rheumatic disorders. It would be worth observing these cases to determine if they are otherwise prone to development of osteoporosis during pregnancy or in later life.(Am J Dis Child 133: [894][895][896][897][898][899][900] 1979) Idi opathi c juvenile osteoporosis is an uncommon self-limited disease that affects previously healthy chil¬ dren. It starts around the ages of 8 to 14 years and is characterized by arrest of growth, loss of height, joint pain, and varying degrees of generalized osteoporosis with vertebral collapse. The children recover spontaneously during later puberty. Teotia1 reported idiopathic juvenile osteoporosis the first time from India. We describe our further experience with the follow-up of these cases and review 27 similar cases reported in the literature.
REPORT OF CASESCase l.-This boy was born in 1956. His prenatal, natal, and postnatal history was noncontributory. He was well and growing normally. He was brought to us in Novem¬ ber 1968 at the age of 12 years with the complaints of low back pain following a 1.8-m fall eight months previously. This constant dull ache was often aggravated by movements of his spine. A detailed dietary evaluation at this stage revealed a daily intake of 2,200 calories, 40 g of protein, 1,022 mg of calcium, and 86 IU of vitamin D. He had a normal appetite. There was no history of nausea, vomiting, recurrent diarrhea, or steatorrhea. There was no history of recent change in weight, altera¬ tion in facial appearance, ankle swelling, muscular weakness, or bleeding tendency. His two brothers (aged 16 and 5 years) and a sister (aged 1 year) were normal. There was no family history of osteogenesis imperfecta or other metabolic bone disor¬ ders.Examination revealed a young boy of average build. His measurements were as follows: height, 127 cm (crown to pubis height, 57.5 cm; pubis to heel height, 69.2 cm), span, 127 cm, and weight, 27.3 kg. Apart from dorsal cyphosis and pigeon chest, no other abnormal findings could be detected on thorough physical examina¬ tion.Results of the following investigations were normal: hemoglobin, total leukocyte count, differential leukocyte count, ESR, electrophoretic strip, serum sodium, serum potassium, serum chloride, serum bilirubin, prothrombin time, urine concentration, and dilution test, and amino acid chromatogram. The plasma calcium value was 9.8 mg/dL; phosphorus, 5.2 mg/dL; alkaline phosphatase, 22 King-Armstrong units/ dL; urinary excretion of calcium, 156 mg/ day; phosphorus excretion, 768 mg/day; 17-ketosteroid excretion, 3.2 mg/day; and 17-ketogenic steroid excretion,...