Kshirsagar Vinayak Y, Ahmed Minhajuddin, Nagarsenkar Suhel, Sahoo Kulmani, Shah Kuldeep B
Department of Pediatrics, Krishna Institute of Medical Sciences, University Krishna Hospital, Karad, Maharashtra, India.
Acta Med Acad. 2012;41(2):214-8. doi: 10.5644/ama2006-124.54.
Pycnodysostosis is a rare autosomal recessive disorder whose gene responsible for this phenotype (CTSK), mapped to human chromosome 1q21, code for the enzyme cathepsin K, a lysosomal cysteine protease; with an estimated incidence of 1.7 per 1 million births. This clinical entity includes micromelic dwarfism, increased radiological bone density, dysplasia of the skull, acro-osteolysis, straightening of the mandibular angle and in some cases, dysplasia of the acromial end of the clavicle. Oral and maxillo-facial manifestations of this disease are very clear. Herein we reported a case of pycnodysostosis, showing short stature with widening of the sutures, unfused anterior and posterior fontanelles, crowding of teeth with dental caries and typical radiological features associated with ichthyosis vulgaris and palmoplantar keratoderma.
致密性成骨不全症是一种罕见的常染色体隐性疾病,其导致该表型的基因(CTSK)定位于人类1号染色体长臂21区,编码组织蛋白酶K,一种溶酶体半胱氨酸蛋白酶;估计发病率为每100万例出生中有1.7例。该临床病症包括短肢侏儒症、放射学骨密度增加、颅骨发育异常、肢端骨质溶解、下颌角变直,在某些情况下还包括锁骨肩峰端发育异常。这种疾病的口腔颌面部表现非常明显。在此我们报告一例致密性成骨不全症病例,表现为身材矮小、缝线增宽、前后囟未闭合、牙齿拥挤伴龋齿以及与寻常型鱼鳞病和掌跖角化病相关的典型放射学特征。