Reddy B S, Thadeus J, Garg B R, Rathnakar C
Departments of Dermatology and STD and Pathology, JIPMER, Pondicherry-605 006, India, .
Indian J Dermatol Venereol Leprol. 1995 Mar-Apr;61(2):106-8.
The case findings in a 22-year-old male patient of keratosis follicularis spinulosa decalvans are described. In addition to the characteristic cutaneous, occular and histological features, he had striking angular stomatitis and fissuring of the tongue simulating vitamin B-complex deficiency. This is an unreported feature to our knowledge. The mode of inheritance suggested X-linked trait.
本文描述了一名22岁男性毛囊角化病性秃发患者的病例发现。除了具有特征性的皮肤、眼部和组织学特征外，他还出现了明显的口角炎和舌裂，类似于复合维生素B缺乏症。据我们所知，这是一个未被报道过的特征。遗传模式提示为X连锁性状。
