This paper is a critical review of the newly published second edition of “Developmental Juvenile Osteology” by C. Cunningham, L. Scheuer and S. Black. It is extensively illustrated by Angela Christie portraying the ...This paper is a critical review of the newly published second edition of “Developmental Juvenile Osteology” by C. Cunningham, L. Scheuer and S. Black. It is extensively illustrated by Angela Christie portraying the developing human skeleton at varying stages of juvenile growth. A chapter on the dentition omits mention of attritional wear or identifies caries restorative materials. Despite an extensive bibliography, failure to provide reference sources detracts from an incomparable source of developmental skeletal enlightenment.展开更多
The 16th National Congress of the Communist Party of China was held inNovember 2002. In the five years since then, great changes took place in Chinesepower industry. Power institutional reform was deepened; the constr...The 16th National Congress of the Communist Party of China was held inNovember 2002. In the five years since then, great changes took place in Chinesepower industry. Power institutional reform was deepened; the construction ofboth power sources and power grids was speeded up; the tense situation of powersupply and demand was alleviated; the safety and reliability of power productionwere improved; the management on power tariff was standardized; environmentalprotection and energy conservation achieved good results; researches on newtechnologies made new achievements; and the operation of enterprises was im-proved.展开更多
Based on the review of the papers and other related material submitted to the conference, the status quo and developmental trends of geocryology is briefly discussed.
Background: With transitions in the disease concept of orthokeratinized odontogenic cyst (OOC), the pathogenesis and etiology have not been sufficiently elucidated. Objectives: OOC cases were reclassified and observed...Background: With transitions in the disease concept of orthokeratinized odontogenic cyst (OOC), the pathogenesis and etiology have not been sufficiently elucidated. Objectives: OOC cases were reclassified and observed to understand the clinico-histopathological characteristics. In addition, literature review of OOC was performed to better organize the pathology. Materials and methods: Subjects with jawbone cysts lined by keratinized stratified squamous epithelium from 2005 to 2018 were reclassified, and clinico-histopathological findings were analyzed. Previous reports of OOC/orthokeratinized-type odontogenic keratocyst (OKC) from 1980 to 2019 were organized. Results: Five cases of OOC were diagnosed, representing 2.1% of odontogenic developmental cysts (total, 239 cases). Mean age was 37.6 years, with a female predominance. The mandibular molar area was the frequent site, and all cysts were solitary. Sixty percent involved an impacted tooth. Mean maximum diameter of the cyst was 2.2 cm. Histopathologically, 4 cases were unilocular, and partial palisading of the basal layer and scattered epithelial islands were observed in 2 cases each and formation of daughter cysts was noted in 3 cases. Previous papers described that most were unilocular and related to impacted teeth. Mean age ranged between 20 and 40 years, and the mandibular molar region was dominant. Recurrence rates were low. Conclusion: OOC shows a different biological attitude to OKC and is closer to dentigerous cyst. Meanwhile, OOC shows a similar histology of epidermoid cysts accompanying the granular layer. We thus surmised that OCC represents an independent concept as an odontogenic developmental cyst.展开更多
该文报道1个累及3代共9人的Nascimento型X连锁智力障碍(Nascimento form of syndromic X-linked intellectual developmental disorder,MRXSN)大家系的临床特点及基因突变类型并进行文献复习。家系中共9人有相似的智力障碍、特殊面容等...该文报道1个累及3代共9人的Nascimento型X连锁智力障碍(Nascimento form of syndromic X-linked intellectual developmental disorder,MRXSN)大家系的临床特点及基因突变类型并进行文献复习。家系中共9人有相似的智力障碍、特殊面容等,其中4人已去世。基因检测提示先证者UBE2A基因存在2~3号外显子缺失,来自母亲。荧光定量聚合酶链反应显示,先证者和表舅UBE2A基因存在2~3号外显子缺失,先证者之母亲、外婆及表姨奶UBE2A基因存在2~3号外显子杂合缺失;先证者之父亲、姐姐、表姨UBE2A基因2~3号外显子拷贝数均正常。文献报道的34例患者临床表型多样,UBE2A基因突变(22/34,65%)和大片段缺失(12/34,35%)为主要突变类型。中重度智力障碍(34/34,100%)、言语障碍(33/34,97%)、特殊面容(32/34,94%)等是MRXSN患者主要的临床表现。该病具有明显的表型异质性,尽早明确诊断有利于优生优育。展开更多
文摘This paper is a critical review of the newly published second edition of “Developmental Juvenile Osteology” by C. Cunningham, L. Scheuer and S. Black. It is extensively illustrated by Angela Christie portraying the developing human skeleton at varying stages of juvenile growth. A chapter on the dentition omits mention of attritional wear or identifies caries restorative materials. Despite an extensive bibliography, failure to provide reference sources detracts from an incomparable source of developmental skeletal enlightenment.
文摘The 16th National Congress of the Communist Party of China was held inNovember 2002. In the five years since then, great changes took place in Chinesepower industry. Power institutional reform was deepened; the construction ofboth power sources and power grids was speeded up; the tense situation of powersupply and demand was alleviated; the safety and reliability of power productionwere improved; the management on power tariff was standardized; environmentalprotection and energy conservation achieved good results; researches on newtechnologies made new achievements; and the operation of enterprises was im-proved.
文摘Based on the review of the papers and other related material submitted to the conference, the status quo and developmental trends of geocryology is briefly discussed.
文摘Background: With transitions in the disease concept of orthokeratinized odontogenic cyst (OOC), the pathogenesis and etiology have not been sufficiently elucidated. Objectives: OOC cases were reclassified and observed to understand the clinico-histopathological characteristics. In addition, literature review of OOC was performed to better organize the pathology. Materials and methods: Subjects with jawbone cysts lined by keratinized stratified squamous epithelium from 2005 to 2018 were reclassified, and clinico-histopathological findings were analyzed. Previous reports of OOC/orthokeratinized-type odontogenic keratocyst (OKC) from 1980 to 2019 were organized. Results: Five cases of OOC were diagnosed, representing 2.1% of odontogenic developmental cysts (total, 239 cases). Mean age was 37.6 years, with a female predominance. The mandibular molar area was the frequent site, and all cysts were solitary. Sixty percent involved an impacted tooth. Mean maximum diameter of the cyst was 2.2 cm. Histopathologically, 4 cases were unilocular, and partial palisading of the basal layer and scattered epithelial islands were observed in 2 cases each and formation of daughter cysts was noted in 3 cases. Previous papers described that most were unilocular and related to impacted teeth. Mean age ranged between 20 and 40 years, and the mandibular molar region was dominant. Recurrence rates were low. Conclusion: OOC shows a different biological attitude to OKC and is closer to dentigerous cyst. Meanwhile, OOC shows a similar histology of epidermoid cysts accompanying the granular layer. We thus surmised that OCC represents an independent concept as an odontogenic developmental cyst.
文摘该文报道1个累及3代共9人的Nascimento型X连锁智力障碍(Nascimento form of syndromic X-linked intellectual developmental disorder,MRXSN)大家系的临床特点及基因突变类型并进行文献复习。家系中共9人有相似的智力障碍、特殊面容等,其中4人已去世。基因检测提示先证者UBE2A基因存在2~3号外显子缺失,来自母亲。荧光定量聚合酶链反应显示,先证者和表舅UBE2A基因存在2~3号外显子缺失,先证者之母亲、外婆及表姨奶UBE2A基因存在2~3号外显子杂合缺失;先证者之父亲、姐姐、表姨UBE2A基因2~3号外显子拷贝数均正常。文献报道的34例患者临床表型多样,UBE2A基因突变(22/34,65%)和大片段缺失(12/34,35%)为主要突变类型。中重度智力障碍(34/34,100%)、言语障碍(33/34,97%)、特殊面容(32/34,94%)等是MRXSN患者主要的临床表现。该病具有明显的表型异质性,尽早明确诊断有利于优生优育。
