Connections between traditional Chinese medicine and congenital syndromes
2001; Wiley; Volume: 103; Issue: 3 Linguagem: Inglês
10.1002/ajmg.1562
ISSN1096-8628
Autores Tópico(s)Tracheal and airway disorders
ResumoAmerican Journal of Medical GeneticsVolume 103, Issue 3 p. 257-262 Letter to the Editor Connections between traditional Chinese medicine and congenital syndromes Jesse Li-Ling, Corresponding Author Jesse Li-Ling [email protected] Institute of Bioinformatics, Tsinghua University, Beijing, ChinaInstitute of Bioinformatics, Room 219, Life Science Building, Tsinghua University, Beijing, 100084 China.Search for more papers by this author Jesse Li-Ling, Corresponding Author Jesse Li-Ling [email protected] Institute of Bioinformatics, Tsinghua University, Beijing, ChinaInstitute of Bioinformatics, Room 219, Life Science Building, Tsinghua University, Beijing, 100084 China.Search for more papers by this author First published: 25 September 2001 https://doi.org/10.1002/ajmg.1562Citations: 6Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat REFERENCES Academy of Traditional Chinese Medicine. 1975. An outline of Chinese acupuncture. Peking: Foreign Language Press. p 33–69. Adkins WY, Gussen R. 1974. Temporal bone findings in the third and fourth pharyngeal pouch (DiGeorge) syndrome. Arch Otolaryngol 100: 206–208. Amati F, Mari A, Digilio MC, Mingarelli R, Marino B, Giannotti A, Novelli G, Dallapiccola B. 1995. 22q11 deletions in isolated and syndromic patients with tetralogy of Fallot. Hum Genet 95: 479–482. Black FO, Spanier SS, Kohut RI. 1975. Aural abnormalities in partial DiGeorge syndrome. Arch Otolaryngol 101: 129–134. Burn J, Goodship J. 1996. Congenital heart disease. In: DL Rimoin, JM O'Conner, RE Pyeritz, editors. Emery and Rimoin's principle and practice of medical genetics, vol. 1, 3rd ed. New York: Churchill Livingstone. p 767–828. Clark EB. 1995. Epidemiology of congenital cardiovascular malformations. In: GC Emmanouilides, HD Allen, TA Riemenschneider, HP Gutgesell, editors. Moss and Adams' heart diseases in infants, children, and adolescents including the fetus and young adults. Baltimore: Williams and Wilkins. p 60–70. Cunningham CK, Weiner LB, Shprintzen RJ. 1997. Respiratory infections in children with velo-cardio-facial syndrome (VCFS). Am J Hum Genet 61 ( Suppl): A95. Deerojanawong J, Chang AB, Eng PA, Robertson CF, Kemp AS. 1997. Pulmonary diseases in children with severe combined immune deficiency and DiGeorge syndrome. Pediatr Pulmonol 24: 324–330. Han-yu Ci-dian. 1937. Chinese dictionary. Hong-Kong: Business Press. p 349. Hofbeck M, Rauch A, Buheitel G, Leipold G, von der Emde J, Pfeiffer R, Singer H. 1998. Monosomy 22q11 in patients with pulmonary atresia, ventricular septal defect, and major aortopulmonary collateral arteries. Heart 79: 180–185. Hofbeck M, Leipold G, Rauch A, Buheitel G, Singer H. 1999. Clinical relevance of monosomy 22q11.2 in children with pulmonary atresia and ventricular septal defect. Eur J Pediatr 158: 302–307. Huang-di Nei-jing Su-wen [Inner classic of the yellow emperor]. 1963 [Reprint]. Beijing: People's Health Press. p 320–321. Iserin L, de Lonlay P, Viot G, Sidi D, Kachaner J, Munnich A, Lyonnet S, Vekemans M, Bonnet D. 1998. Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomalies. Eur J Pediatr 157: 881–884. Johnson MC, Strauss AW, Dowton SB, Spray TL, Huddleston CB, Wood MK, Slaugh RA, Watson MS. 1995. Deletion within chromosome 22 is common in patients with absent pulmonary valve syndrome. Am J Cardiol 76: 66–69. Kaptchuk TJ. 1983. Chinese medicine, the web that has no weaver. London: Rider. p 35–114. Kerstjens-Frederikse WS, Kurahashi HR, van Essen AJ. 1999. A Hirschsprung disease locus at 22q11? J Med Genet 36: 221–224. Lewin MB, Lindsay EA, Jurecic V, Goytia V, Towbin JA, Baldini A. 1997. A genetic etiology for interruption of the aortic arch type B. Am J Cardiol 80: 493–497. Lu G-D, Needham J. 1980. Celestial lancet, a history and rationale of acupuncture and moxa. Cambridge: Cambridge University Press. 17 p. Martinez-Frias ML. 1995. Primary midline developmental field. I. Clinical and epidemiological characteristics. Am J Med Genet 56: 374–381. Matsuoka R, Kimura M, Scambler PJ, Morrow BE, Imamura S, Minoshima S, Shimizu N, Yamagishi H, Joh-o K, Watanabe S, Oyama K, Saji T, Ando M, Takao A, Momma K. 1998. Molecular and clinical study of 183 patients with conotruncal anomaly face syndrome. Hum Genet 103: 70–80. McDonald-McGinn DM, Kirschner R, Goldmuntz E, Sullivan K, Eicher P, Gerdes M, Moss E, Solot C, Wang P, Jacobs I, Handler S, Knightly C, Heher K, Wilson M, Ming JE, Grace K, Driscoll D, Pasquariello P, Randall P, LaRossa D, Emanuel BS, Zackai EH. 1999. The Philadelphia story: the 22q11.2 deletion: report on 250 patients. Genet Couns 10: 11–24. Mehraein Y, Wippermann CF, Michel-Behnke I, Nhan Ngo TK, Hillig U, Giersberg M, Aulepp U, Barth H, Fritz B, Rehder H. 1997. Microdeletion 22q11 in complex cardiovascular malformations. Hum Genet 99: 433–442. Ming JE, McDonald-McGinn DM, Megerian TE, Driscoll DA, Elias ER, Russell BM, Irons M, Emanuel BS, Markowitz RI, Zackai EH. 1997. Skeletal anomalies and deformities in patients with deletions of 22q11. Am J Med Genet 72: 210–215. Mitnick RJ, Bello JA, Shprintzen RJ. 1994. Brain anomalies in velo-cardio-facial syndrome. Am J Med Genet 54: 100–106. Morse MJ, Lirenman DS, Johnson HW. 1981. The association of renal pelviocaliceal dysmorphism with sensorineural deafness: a new syndrome. J Urol 125: 625–627. Nakada K, Kawaguchi F, Wakisaka M, Nakada M, Enami T. 1997. Digestive tract disorders associated with asplenia/polysplenia syndrome. J Pediatr Surg 32: 91–94. Ni M. 1995. The yellow emperor's classic of medicine. Boston: Shambhala. 16 p. Ohtani I, Schuknecht HF. 1984. Temporal bone pathology in DiGeorge's syndrome. Ann Otol Rhinol Laryngol 93: 220–224. Opitz JM. 1985. The development field concept. Am J Med Genet 21: 1–11. Osborne J, Masel J, McCredie J. 1989. A spectrum of skeletal anomalies associated with pulmonary agenesis: possible neural crest injuries. Pediatr Radiol 19: 425–432. Penman Splitt M, Burn J, Goodship J. 1996. Defects in the determination of left-right asymmetry. J Med Genet 33: 498–503. Perry LW. 1993. The Baltimore-Washington infant heart study. In: C Ferencz, editor. Epidemiology of CHD. Mount Kisco, NY: Futura Publishing Co., Inc. p 33–61. Recto MR, Parness IA, Gelb BD, Lopez L, Lai WW. 1997. Clinical implications and possible association of malposition of the branch pulmonary arteries with DiGeorge syndrome and microdeletion of chromosome region 22q11. Am J Cardiol 80: 1624–1627. Rommel N, Vantrappen G, Swillen A, Devriendt K, Feenstra L, Fryns JP. 1999. Retrospective analysis of feeding and speech disorders in 50 patients with velo-cardio-facial syndrome. Genet Couns 10: 104. Ryan AK, Goodship JA, Wilson DI, Philip N, Levy A, Seidel H, Schuffenhauer S, Oechsler H, Belohradsky B, Prieur M, Aurias A, Raymond FL, Clayton-Smith J, Hatchwell E, McKeown C, Beemer FA, Dallapiccola B, Novelli G, Hurst JA, Ignatius J, Green AJ, Winter RM, Brueton L, Brondum-Nielsen K, Scambler PJ. 1997. Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study. J Med Genet 34: 798–804. Schmidt JM. 1985. Cochlear neuronal populations in developmental defects of the inner ear. Implications for cochlear implantation. Acta Otolaryngeal (Stockh) 99: 14–20. Shprintzen R. 1999. The ENT manifestations of velo-cardio-facial syndrome. Genet Couns 10: 103–104. Swillen A, Devriendt K, Legius E, Prinzie P, Vegels A, Ghesquiere P, Fryns JP. 1999. The behaviour phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence. Genet Couns 10: 79–88. Tewfik TL, Teebi AS, der Kaloustian VM. 1997. Syndromes and conditions associated with congenital anomalies of the ear. In: TL Tewfik, VM der Kaloustian, editors. Congenital anomalies of the ear, nose and throat. New York: Oxford University Press. van Mierop LH, Kutsche LM. 1986. Cardiovascular anomalies in DiGeorge syndrome and importance of neural crest as a possible pathogenetic factor. Am J Cardiol 58: 133–137. Verloes A, Curry C, Jamar M, Herens C, O'Lague P, Marks J, Sarda P, Blanchet P. 1998. Juvenile rheumatoid arthritis and del(22q11) syndrome: a non-random association. J Med Genet 35: 943–947. Wilson DI, Goodship JA, Burn J, Cross IE, Scambler PJ. 1992. Deletions within chromosome 22q11 in familial congenital heart disease. Lancet 340: 573–575. Winter RM, Baraitser M. 1991. Multiple congenital anomalies: a diagnostic compendium. London, New York: Chapman and Hall Medical. p 283–284. Worthington S, Colley A, Fagan K, Dai K, Lipson AH. 1997. Anal anomalies: an uncommon feature of velocardiofacial (Shprintzen) syndrome? J Med Genet 34: 79–82. Citing Literature Volume103, Issue315 October 2001Pages 257-262 ReferencesRelatedInformation
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