Warkany syndrome 1

In this article, we will explore Warkany syndrome 1 in depth, a topic that has sparked much interest and debate in recent years. From its origins to its impact on today's society, we will examine all aspects related to Warkany syndrome 1 to provide a comprehensive and complete overview. Through interviews, research and analysis, we will seek to better understand this topic and its influence on different areas of daily life. From its relevance in academia to its role in popular culture, Warkany syndrome 1 has captured the attention of many and has generated a series of questions and concerns that we will try to address in this article. Join us on this journey of discovery and learning about Warkany syndrome 1!

Warkany syndrome

Warkany syndrome 1 was an X-chromosome linked recessive genetic condition originally described by Joseph Warkany in 1961 as part of an article on intrauterine growth retardation[1] - the condition is no longer diagnosed. The family history was consistent with X-linked recessive inheritance of intrauterine growth retardation and small head size, but these features are not unique to this condition and no linkage to a specific gene was ever established. In fact, the condition appears to have been abandoned, given that the OMIM number (308400) assigned to it () and listed in a review article on X-linked mental retardation[2] has been removed from the OMIM database. Furthermore, this condition is no longer mentioned in a more recent review of X-linked mental retardation.[3]

See also

References

  1. ^ Warkany J (1961). "Intrauterine growth retardation". Am. J. Dis. Child. 102 (2): 249–79. doi:10.1001/archpedi.1961.02080010251018. PMID 13783175.
  2. ^ Lubs H (1999). "XLMR genes: update 1998". Am. J. Med. Genet. 83 (4): 237–47. doi:10.1002/(SICI)1096-8628(19990402)83:4<237::AID-AJMG2>3.0.CO;2-8. PMID 10208155.
  3. ^ Chiurazzi P (2008). "XLMR genes: update 2007". Eur. J. Hum. Genet. 16 (4): 422–34. doi:10.1038/sj.ejhg.5201994. PMID 18197188.


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