Fraccaro Syndrome: Report of Two Iranian Cases: An Infant and an Adult in A Family Fraccaro Syndrome...
Fraccaro Syndrome: Report of Two Iranian Cases: An Infant and an Adult in A Family Fraccaro Syndrome: Report of Two Iranian Cases: An Infant and an Adult in A Family
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Publisher
Tehran University of Medical Sciences
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Language
English
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Publisher
Tehran University of Medical Sciences
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Contents
49,XXXXY is rare chromosomal pattern and these patients have mental retardation, small penis, cryptorchidism and skeletal anomalies. We reported a 10 month-old boy who has hypotonia, microcephaly, hypertelorism, depressed nasal bridge, epicanthic folds and bilateral multiple ear tags, high arched palate, down set ears, micrognathia and congenital h...
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Full title
Fraccaro Syndrome: Report of Two Iranian Cases: An Infant and an Adult in A Family Fraccaro Syndrome: Report of Two Iranian Cases: An Infant and an Adult in A Family
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TN_cdi_doaj_primary_oai_doaj_org_article_5afb108a86f34f0b9c1e8699df67bf38
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_5afb108a86f34f0b9c1e8699df67bf38
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ISSN
0044-6025
E-ISSN
1735-9694
