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Neuroectodermal (CHIME) syndrome: an additional case with long term follow up of all reported cases.
J Med Genet. 1995 Jun;32(6):465-9. doi: 10.1136/jmg.32.6.465.
J Med Genet. 1995.
PMID: 7666399
Free PMC article.
Review.
A new neuroectodermal syndrome (designated CHIME syndrome) was described in 1983 with a total of four patients reported, it is presumed to be an autosomal recessive disorder because of recurrence in sibs. ...
A new neuroectodermal syndrome (designated CHIME syndrome) was described in 1983 with a total of four patients reported, it is …
Acute lymphoblastic leukemia in a child with the CHIME neuroectodermal dysplasia syndrome.
Schnur RE, Greenbaum BH, Heymann WR, Christensen K, Buck AS, Reid CS.
Schnur RE, et al.
Am J Med Genet. 1997 Oct 3;72(1):24-9.
Am J Med Genet. 1997.
PMID: 9295069
Review.
The "CHIME" syndrome (MIM#280000) is a rare neuroectodermal disorder comprised of Colobomas of the eye, Heart defects, Ichthyosiform dermatosis, Mental retardation, and Ear defects. ...Histologic examination of the skin demonstrated findings of an epidermal nevus wi …
The "CHIME" syndrome (MIM#280000) is a rare neuroectodermal disorder comprised of Colobomas of the eye, Heart defects, Ichthyo …
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