Realizing “carbon peaking” and “carbon neutrality” is a major strategic decision made by China to coordinate domestic and international situations.In order to achieve the “double carbon” goal,it is also necessar...Realizing “carbon peaking” and “carbon neutrality” is a major strategic decision made by China to coordinate domestic and international situations.In order to achieve the “double carbon” goal,it is also necessary for relevant practitioners to actively put into practice to improve the participation of residents and advocate low carbon life while formulating the policy action plan.Community is an important place for human activities and one of the main spatial types of carbon emissions in cities.Doing a good job in planning energy conservation and emission reduction in the community plays an important role in achieving the “double carbon” goal.Through the analysis of classic low carbon community practice cases at home and abroad,6 planning and design methods for low carbon community are concluded,and the development status of low carbon community in China is reflected and summarized.展开更多
Bardet-Biedl Syndrome (BBS) is a rare autosomal recessive ciliopathy characterized by obesity, post-axial polydactyly, renal abnormalities, mental retardation, pigmentary retinopathy and hypogenitalism. Diagnosis is r...Bardet-Biedl Syndrome (BBS) is a rare autosomal recessive ciliopathy characterized by obesity, post-axial polydactyly, renal abnormalities, mental retardation, pigmentary retinopathy and hypogenitalism. Diagnosis is rare in early childhood, and only few of the features are present at that age. This is because the disease is slow evolving. However, it is possible to find majority of the component of this syndrome in very young children. A 3-year old very obese male presented with clinical features of sepsis and congestive cardiac failure. He is a product of non-consanguineous marriage with unremarkable family history. Both parents are of the Ibo tribe in Nigeria. Polydactyly was noticed at birth. There was delay in some aspects of his developmental milestone. Examination revealed mild hypertelorism and retrognathia, polydactyly of both feet with syndactyly of the big and second toes. Other findings were short broad hands, mottled pigments on the retina, moderate mental retardation, hypogenitalism, nephrotic syndrome, renal tubulopathy, hyperglycaemia and hypopigmented skin lesions. A case of BBS with all the primary features and some secondary manifestations in a very young child is hereby reported. A high index of suspicion for BBS should be shown in any young child with at least one of the features of this syndrome. This will enhance earlier diagnosis and improve disease outcome.展开更多
基金Sponsored by General Project of Natural Science Foundation of Beijing (8202017)Youth Talent Support Program of 2018 Beijing Municipal University Academic Human Resources Development (PXM2018_014212_000043)。
文摘Realizing “carbon peaking” and “carbon neutrality” is a major strategic decision made by China to coordinate domestic and international situations.In order to achieve the “double carbon” goal,it is also necessary for relevant practitioners to actively put into practice to improve the participation of residents and advocate low carbon life while formulating the policy action plan.Community is an important place for human activities and one of the main spatial types of carbon emissions in cities.Doing a good job in planning energy conservation and emission reduction in the community plays an important role in achieving the “double carbon” goal.Through the analysis of classic low carbon community practice cases at home and abroad,6 planning and design methods for low carbon community are concluded,and the development status of low carbon community in China is reflected and summarized.
文摘Bardet-Biedl Syndrome (BBS) is a rare autosomal recessive ciliopathy characterized by obesity, post-axial polydactyly, renal abnormalities, mental retardation, pigmentary retinopathy and hypogenitalism. Diagnosis is rare in early childhood, and only few of the features are present at that age. This is because the disease is slow evolving. However, it is possible to find majority of the component of this syndrome in very young children. A 3-year old very obese male presented with clinical features of sepsis and congestive cardiac failure. He is a product of non-consanguineous marriage with unremarkable family history. Both parents are of the Ibo tribe in Nigeria. Polydactyly was noticed at birth. There was delay in some aspects of his developmental milestone. Examination revealed mild hypertelorism and retrognathia, polydactyly of both feet with syndactyly of the big and second toes. Other findings were short broad hands, mottled pigments on the retina, moderate mental retardation, hypogenitalism, nephrotic syndrome, renal tubulopathy, hyperglycaemia and hypopigmented skin lesions. A case of BBS with all the primary features and some secondary manifestations in a very young child is hereby reported. A high index of suspicion for BBS should be shown in any young child with at least one of the features of this syndrome. This will enhance earlier diagnosis and improve disease outcome.
