Breytenbach H S, Gericke G S, Muller C J, Nortjé C J, Shanley B C, Swart E, Van Wyk C W
S Afr Med J. 1975 Mar 29;49(14):544-50.
The clinical, genetic, radiological, dental and dermatological aspects of 3 patients with the autosomal dominant basal cell naevus syndrome are reported. An analysis of the phenotypic features of 72 cases described in the literature is presented and compared with a previous analysis. Ash leaf hypopigmentation similar to that found in tuberous sclerosis represents a unique finding in this syndrome. Other similarities to the phacomatoses are discussed. We were able to support a previous report that patients with the basal cell naevus syndrome have a normal end-organ response to parathormone stimulation, and that it is most probably not related to pseudohypoparathyroidism, as earlier reports suggested.
报告了3例常染色体显性遗传性基底细胞痣综合征患者的临床、遗传、放射学、牙科和皮肤病学方面的情况。对文献中描述的72例病例的表型特征进行了分析,并与之前的分析进行了比较。类似于结节性硬化症中发现的树叶状色素减退是该综合征的一个独特表现。还讨论了与母斑病的其他相似之处。我们能够支持之前的一份报告,即基底细胞痣综合征患者对甲状旁腺激素刺激的终末器官反应正常,而且很可能与之前报告所暗示的假甲状旁腺功能减退无关。