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pubmed-article:2764029pubmed:abstractTextWe report on a patient, born to consanguineous parents, who had a complex malformation syndrome of severe upper limbs anomalies, peculiar face, structural ear anomalies, nasolacrimal duct obstruction, and abnormal hair and nails. We think that the clinical manifestations of the patient are similar to those described by Freire-Maia as the odontotrichomelic syndrome; the differential diagnosis between this syndrome and ectrodactyly, ectodermal dysplasia, and cleft/lip palate (EEC) syndrome is discussed.lld:pubmed
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pubmed-article:2764029pubmed:dateRevised2004-11-17lld:pubmed
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pubmed-article:2764029pubmed:year1989lld:pubmed
pubmed-article:2764029pubmed:articleTitleA case of the Freire-Maia Odontotrichomelic syndrome: nosology with EEC syndrome.lld:pubmed
pubmed-article:2764029pubmed:affiliationClinica Pediatrica, Università di Catania, Italy.lld:pubmed
pubmed-article:2764029pubmed:publicationTypeJournal Articlelld:pubmed
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