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Clin Pediatr (Phila) ; 14(4): 355-7/362-8, 1975 Apr.
Article in English | MEDLINE | ID: mdl-164311

ABSTRACT

A high percentage of Greek children with homozygous b-thalassemia were short and had a lag in growth, though some severely affected attained normal height. Bone age lagged significantly behind the chronologic age, even in those with normal height for their age. A longitudinal study demonstrated an initial normal growth velocity which decreased after the age of six for males and eight for females. No patient had a spurt of growth at adolescence. Height gain continued up to the age of 21 and then ceased. Statistical analysis with a multiple regression equation showed a significant relationship between the age and height of the patients. Low hemoglobin levels and severity of the disease seemed to hinder normal growth, but neither relationship was statistically significant.


Subject(s)
Body Height , Growth Disorders/etiology , Thalassemia/complications , Adolescent , Adult , Age Determination by Skeleton , Age Factors , Child , Child, Preschool , Female , Greece , Hemoglobins/analysis , Homozygote , Humans , Infant , Male , Regression Analysis , Thalassemia/blood , Thalassemia/physiopathology
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