Congenital hypopituitarism and multiple midline defects in a newborn with non-familial Cat Eye syndrome
Abstract Background Cat eye syndrome (CES) is a rare chromosomal disease, with estimated incidence of about 1 in 100,000 live newborns. The classic triad of iris coloboma, anorectal malformations, and auricular abnormalities is present in 40% of patients, and other congenital defects may also be obs...
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| Main Authors: | , , , , , , , , , , , , |
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| Format: | Book |
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BMC,
2022-09-01T00:00:00Z.
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