Etiopathogenesis of craniosynostosis.

M. M. Cohen

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

Etiopathogenesis of craniosynostosis.

M. M. Cohen

Medicine

Résultat de recherche: Review article › examen par les pairs

66 Citations (Scopus)

Résumé

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).

Langue d'origine	English
Pages (de-à)	507-513
Nombre de pages	7
Journal	Neurosurgery Clinics of North America
Volume	2
Numéro de publication	3
DOI	https://doi.org/10.1016/s1042-3680(18)30714-9
Statut de publication	Published - juill. 1991

ASJC Scopus Subject Areas

Surgery
Clinical Neurology

PubMed: MeSH publication types

Journal Article
Review

Accès au document

10.1016/s1042-3680(18)30714-9

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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.

Résumé

ASJC Scopus Subject Areas

PubMed: MeSH publication types

Accès au document

Autres fichiers et liens

Empreinte numérique

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