Laron Z, Roitman A, Kauli R
Clin Endocrinol (Oxf). 1979 Apr;10(4):393-9. doi: 10.1111/j.1365-2265.1979.tb02094.x.
Head circumference was measured before and during hGH therapy in fourteen children with isolated growth hormone deficiency (IGHD) and in twenty-one children with multiple pituitary hormone deficiencies (MPHD). In both groups there was a retardation in growth of the neurocranium, more marked in the children with IGHD, which was less than the retardation in linear height. In the group with IGHD, initiation of hGH therapy before a chronological age of 5 and a bone age of 3 had been reached led to a rapid catch-up in cranial growth with normalization of the head size. In older children the induction of head growth was similar to that achieved by the long bones but without a true catch-up phenomenon. In three adults with hereditary IGHD without therapy or with irregular treatment during late puberty, the head circumference was below normal range. In view of the possible role played by development of brain tissue upon cranial size, the importance of early diagnosis and initiation of therapy in infants and young children with a deficiency of hGH is stressed.
对14名孤立性生长激素缺乏症(IGHD)患儿和21名多种垂体激素缺乏症(MPHD)患儿在生长激素(hGH)治疗前及治疗期间测量了头围。两组患儿的神经颅骨生长均迟缓,IGHD患儿更为明显,且小于线性身高的迟缓程度。在IGHD组中,在实际年龄达到5岁且骨龄达到3岁之前开始hGH治疗,可导致颅骨生长迅速追赶,头围恢复正常。在年龄较大的儿童中,头部生长的诱导与长骨相似,但没有真正的追赶现象。在3名患有遗传性IGHD且在青春期后期未接受治疗或治疗不规律的成年人中,头围低于正常范围。鉴于脑组织发育对颅骨大小可能起到的作用,强调了对hGH缺乏的婴幼儿进行早期诊断和开始治疗的重要性。