Bone changes in congenital cytomegalic inclusion disease.

Author:

McCandless A E,Davis C,Hall E G

Publisher

BMJ

Subject

Pediatrics, Perinatology and Child Health

Reference5 articles.

1. Rubella-like bone changes in congenital cytomegalic inclusion disease;Graham, C.B.; Thal, A.; Wassum, C.S.;Radiology,1970

2. Skeletal manifestations of congenital cytomegalic inclusion disease;Merton, D.F.; Gooding, C.A.;Radioloqy,1970

3. The roentgenographic manifestations of the rubella syndrome in newborn infants;Singleton, E.B.; Rudolph, A.J.; Rosenberg, H.S.; Singer, D.B.;American Journal of Roenm,1966

4. A girl was born in July 1959. Until the age of 6 years she was well. At this time she began to get frequent bouts of abdominal pain and loose stools. Investigations showed an iron deficiency anaemia. This was treated with oral iron but the response was poor

5. Early in 1973 she noticed that her stool frequency was increasing, and that she was experiencing abdominal pain unlike that which occurred when she ate glutencontaining foods. The rate of her weight gain diminished, and on direct questioning she admitted to heat intolerance, lassitude, and a voracious appetite. Physical examination showed a diffuse goitre over which a bruit could be heard. She had a tachycardia that per-

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