Stamp T C, Baker L R
Arch Dis Child. 1976 May;51(5):360-5. doi: 10.1136/adc.51.5.360.
Two out of 3 children of a first-cousin marriage presented with severe rickets in infancy and are now adult. Their disease has shown continued activity, marked resistance to treatment with vitamin D, early fusion of cranial sutures, greatly increased bone density, nerve deafness, and life-long hypophosphataemia unaffected by treatment. Both parents and a third sib were normal clinically and biochemically. Blood grouping supported both stated paternity and parental consanguinity. Genetics of this unique disease can only be explained satisfactorily on the basis of autosomal recessive transmission, a mode not previously reported in primary hypophosphataemia. This homozygous disease resembles an exaggerated form of common X-linked rickets, though it is caused by a different gene. Although rare, it is particularly important because of the information it provides on the pathogenesis of both forms. We propose that both syndromes may result from multiple target organ unresponsiveness to 1,25-dihydroxycholecalciferol in intestine, kidney, bone, and parathyroid gland.
近亲结婚夫妇所育子女中,三分之二在婴儿期出现严重佝偻病,现已成年。他们的病情持续发展,对维生素D治疗有明显抵抗,颅缝过早融合,骨密度大幅增加,神经性耳聋,且终身低磷血症,治疗无效。父母及第三个孩子临床和生化检查均正常。血型检测证实了所述的亲子关系及父母的血缘关系。这种独特疾病的遗传学特征只能基于常染色体隐性遗传来圆满解释,这种遗传方式在原发性低磷血症中此前未见报道。这种纯合子疾病类似于常见的X连锁佝偻病的一种严重形式,尽管它由不同基因引起。虽然罕见,但因其提供了两种形式的发病机制信息而尤为重要。我们认为,这两种综合征可能都是由于肠道、肾脏、骨骼和甲状旁腺等多个靶器官对1,25 - 二羟胆钙化醇无反应所致。