Etiopathogenesis of craniosynostosis.

M. M. Cohen

doi:10.1016/s1042-3680(18)30714-9

Etiopathogenesis of craniosynostosis.

M. M. Cohen

Medicine

Research output: Contribution to journal › Review article › peer-review

66 Citations (Scopus)

Abstract

Craniosynostosis is both etiologically and pathogenetically heterogeneous. Known causes include monogenic and chromosomal disorders, fetal head constraint, teratogens (aminopterin, diphenylhydantoin, retinoic acid, valproic acid), metabolic diseases (hyperthyroidism, rickets, mucopolysaccharidoses, mucolipidoses), hematologic disorders (thalassemias, sickle cell anemia, congenital hemolytic icterus, polycythemia vera), and malformations (microcephaly, encephalocele, shunted hydrocephaly, holoprosencephaly).

Original language	English
Pages (from-to)	507-513
Number of pages	7
Journal	Neurosurgery Clinics of North America
Volume	2
Issue number	3
DOIs	https://doi.org/10.1016/s1042-3680(18)30714-9
Publication status	Published - Jul 1991

ASJC Scopus Subject Areas

Surgery
Clinical Neurology

PubMed: MeSH publication types

Journal Article
Review

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10.1016/s1042-3680(18)30714-9

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abstract = "Craniosynostosis is both etiologically and pathogenetically heterogeneous. Known causes include monogenic and chromosomal disorders, fetal head constraint, teratogens (aminopterin, diphenylhydantoin, retinoic acid, valproic acid), metabolic diseases (hyperthyroidism, rickets, mucopolysaccharidoses, mucolipidoses), hematologic disorders (thalassemias, sickle cell anemia, congenital hemolytic icterus, polycythemia vera), and malformations (microcephaly, encephalocele, shunted hydrocephaly, holoprosencephaly).",

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AB - Craniosynostosis is both etiologically and pathogenetically heterogeneous. Known causes include monogenic and chromosomal disorders, fetal head constraint, teratogens (aminopterin, diphenylhydantoin, retinoic acid, valproic acid), metabolic diseases (hyperthyroidism, rickets, mucopolysaccharidoses, mucolipidoses), hematologic disorders (thalassemias, sickle cell anemia, congenital hemolytic icterus, polycythemia vera), and malformations (microcephaly, encephalocele, shunted hydrocephaly, holoprosencephaly).

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Etiopathogenesis of craniosynostosis.

Abstract

ASJC Scopus Subject Areas

PubMed: MeSH publication types

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