Human Phenome based on traditional Chinese medicine--a solution to congenital syndromology.

The occurrence of many congenital syndromes has long been an enigma. Clinically, the phenotype of any given genetic defect usually varies to some extent, whilst, pathogenetically, features within each syndrome are probably interconnected, albeit by largely unknown mechanisms. Through its unique theories such as the Jing-Mai (variously translated as the Channels, Vessels or Meridians), Zang-Fu (the Yin and Yang internal organs) and Wu-Xing (translated as the Five-Phase Correspondence or Five-Element theory), traditional Chinese medicine (TCM) seems to have comprehensively summarized the makeup of the human phenotypes. By combining the above TCM theories with modem medical knowledge, the intrinsic mechanisms between various aspects of the phenotypic makeup of the human individual, i.e. the Human Phenome, may be deduced. Analysis of congenital syndromes in light of the Human Phenome seems to suggest that various genetic defects may cause diseases in a similar fashion; i.e. primarily with structural abnormalities distributed along the four Jing-Mai connected with the Kidneys (midline defects) as well as "Marrow" aberrations (anomalies of hematology/immunology, endocrine, central nervous system and the bones). The derived Human Phenome may thereby enable a better understanding of such conditions and provide a model for the study of multigenic traits. On the other hand, blind spots of clinical observation and unknown aspects of human nature, e.g. circuits formed by the JingMai, symmetries of the Jing-Mai and Zang-Fu, and correspondences between body physiques, spiritual factors and the external world may also be deduced. The TCM-based Human Phenome may thereby offer a fresh view for genotype-phenotype correlations, insights into genedevelopment mechanisms, as well as potential directions for the development of new treatments.

[1]  T. Kaptchuk The Web That Has No Weaver : Understanding Chinese Medicine , 1983 .

[2]  J. Opitz,et al.  Errors of morphogenesis: concepts and terms. Recommendations of an international working group. , 1982, The Journal of pediatrics.

[3]  R. Schmickel Contiguous gene syndromes: a component of recognizable syndromes. , 1986, The Journal of pediatrics.

[4]  J. Opitz,et al.  Recommendations of an International Working Group , 1982 .

[5]  中国中医研究院鍼灸研究所 An outline of Chinese acupuncture , 1975 .

[6]  J. Li-Ling,et al.  Connections between traditional Chinese medicine and congenital syndromes. , 2001, American journal of medical genetics.

[7]  G. Verellen,et al.  Association of bilateral renal agenesis and Di George syndrome in an infant of a diabetic mother. , 1982, Helvetica paediatrica acta.

[8]  M. Cohen The Child with Multiple Birth Defects , 1982 .

[9]  B. Emanuel,et al.  Progress in the autosomal segmental aneusomy syndromes (SASs): single or multi-locus disorders? , 1997, Human molecular genetics.

[10]  L. V. van Mierop,et al.  Cardiovascular anomalies in DiGeorge syndrome and importance of neural crest as a possible pathogenetic factor. , 1986, The American journal of cardiology.

[11]  J. Opitz,et al.  The DiGeorge anomaly as a developmental field defect. , 1986, American journal of medical genetics. Supplement.

[12]  H. Langevin,et al.  Relationship of acupuncture points and meridians to connective tissue planes , 2002, The Anatomical record.

[13]  K. Devriendt,et al.  The phenotypic spectrum of the 10p deletion syndrome versus the classical DiGeorge syndrome. , 1999, Genetic counseling.

[14]  J. Opitz,et al.  The developmental field concept. , 1985, American journal of medical genetics.

[15]  Roger H. Reeves Recounting a genetic story , 2000, Nature.

[16]  M. Digilio,et al.  Maternal diabetes causing DiGeorge anomaly and renal agenesis. , 1995, American journal of medical genetics.

[17]  J. Li-Ling,et al.  The Jing-Mai connections of the heart. , 2003, International journal of cardiology.