Trigonocephaly: A new familial syndrome

Trigonocephaly was found in six relatives through three generations of one family. The propositus was ascertained at birth because of omphalocele. In addition to trigonocephaly, he had minor ear, vertebral, and genital abnormalities. His father had mild microcephaly, and both had minor eye abnormali...

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Veröffentlicht in:	American journal of medical genetics 1984-05, Vol.18 (1), p.55-59
Hauptverfasser:	Frydman, Moshe, Kauschansky, Arieh, Elian, Ezra, Opitz, John M.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult autosomal dominant inheritance (trigonocephaly) Biological and medical sciences Child, Preschool Craniosynostoses - genetics craniosynostosis Genes, Dominant Humans Male Malformations of the nervous system Medical sciences metopic suture Neurology omphalocele Pedigree Sex Factors Skull - abnormalities skull deformity Syndrome
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