Craniosynostoses [kraniosynostózy]

topical
56
Terms

akrocefalus
brachycefalus
kraniosynostóza typ 1
metopická synostóza
okcipitální plagiocefalie
okcipitální plagiocefalus
oxycefalus
sagitální synostóza
skafocefalie
skafocefalus
synostotická čelní plagiocefalie
synostotická frontální plagiocefalie
synostotická okcipitální plagiocefalie
synostotický čelní plagiocefalus
synostotický frontální plagiocefalus
synostotický okcipitální plagiocefalus
synostóza koronárního švu
synostóza lambdového švu
synostóza metopického švu
trigonocefalie
trigonocefalus

 

Acrocephaly
Brachycephaly
Craniostenosis
Craniosynostosis
Craniosynostosis, Lambdoidal
Craniosynostosis, Type 1
Lambdoid Synostosis
Metopic Synostosis
Oxycephaly
Plagiocephaly, Craniosynostosis
Plagiocephaly, Synostotic
Sagittal Synostosis
Scaphocephaly
Synostotic Anterior Plagiocephaly
Synostotic Posterior Plagiocephaly
Trigonocephaly
Unilateral Coronal Synostosis

Persistent link   https://www.medvik.cz/link/D003398
Definition

Premature closure of one or more CRANIAL SUTURES. It often results in plagiocephaly. Craniosynostoses that involve multiple sutures are sometimes associated with congenital syndromes such as ACROCEPHALOSYNDACTYLIA; and CRANIOFACIAL DYSOSTOSIS.

DUI
D003398 MeSH Browser
CUI
M0005288
History note
OXYCEPHALY was see under CRANIOSYNOSTOSES 1963-78
Online note
use CRANIOSYNOSTOSES to search OXYCEPHALY 1966-78
Public note
OXYCEPHALY was see under CRANOPSYNOSTOSES 1963-78

C Diseases
C05.116 Bone Diseases 796
C05.116.099.370 Dysostoses 22
C05.116.099.370.894 Synostosis 30
C05.116.099.370.894.115 Antley-Bixler Syndrome Phenotype 1
C05.116.099.370.894.232 Craniosynostoses 56
C05.116.099.370.894.232.015 Acrocephalosyndactylia 10
C05.116.099.370.894.819 Syndactyly 24
C05.116.099.370.894.909 Tarsal Coalition 2
C05.660.207.103 22q11 Deletion Syndrome 2
C05.660.207.207 Cleidocranial Dysplasia 7
C05.660.207.219 Costello Syndrome 3
C05.660.207.231 Craniofacial Dysostosis 28
C05.660.207.240 Craniosynostoses 56
C05.660.207.240.100 Acrocephalosyndactylia 10
C05.660.207.325 Donohue Syndrome 1
C05.660.207.410 Holoprosencephaly 9
C05.660.207.525 LEOPARD Syndrome 11
C05.660.207.532 Loeys-Dietz Syndrome 7
C05.660.207.536 Megalencephaly 7
C05.660.207.620 Microcephaly 78
C05.660.207.690 Noonan Syndrome 52
C05.660.207.700 Orofaciodigital Syndromes 7
C05.660.207.707 Plagiocephaly 3
C05.660.207.720 Platybasia 12
C05.660.207.850 Rubinstein-Taybi Syndrome 12
C05.660.207.925 Silver-Russell Syndrome 3
C05.660.906 Synostosis 30
C05.660.906.364 Craniosynostoses 56
C05.660.906.364.100 Acrocephalosyndactylia 10
C05.660.906.819 Syndactyly 24
C05.660.906.909 Tarsal Coalition 2
C16.131.621.207 Craniofacial Abnormalities 82
C16.131.621.207.103 22q11 Deletion Syndrome 2
C16.131.621.207.207 Cleidocranial Dysplasia 7
C16.131.621.207.231 Craniofacial Dysostosis 28
C16.131.621.207.240 Craniosynostoses 56
C16.131.621.207.240.100 Acrocephalosyndactylia 10
C16.131.621.207.410 Holoprosencephaly 9
C16.131.621.207.525 LEOPARD Syndrome 11
C16.131.621.207.532 Megalencephaly 7
C16.131.621.207.540 Maxillofacial Abnormalities 28
C16.131.621.207.620 Microcephaly 78
C16.131.621.207.690 Noonan Syndrome 52
C16.131.621.207.700 Orofaciodigital Syndromes 7
C16.131.621.207.707 Plagiocephaly 3
C16.131.621.207.720 Platybasia 12
C16.131.621.207.850 Rubinstein-Taybi Syndrome 12
C16.131.621.906 Synostosis 30
C16.131.621.906.364 Craniosynostoses 56
C16.131.621.906.364.100 Acrocephalosyndactylia 10
C16.131.621.906.819 Syndactyly 24
C16.131.621.906.909 Tarsal Coalition 2

Aurocephalosyndactyly Disease MeSH Browser

Baraitser Rodeck Garner syndrome Disease MeSH Browser

Bohring syndrome Disease MeSH Browser

Calabro syndrome Disease MeSH Browser

Cole Carpenter syndrome Disease MeSH Browser

Cranioectodermal Dysplasia Disease MeSH Browser

Craniometaphyseal dysplasia, autosomal recessive type Disease MeSH Browser

Craniosynostosis Mental Retardation Clefting Syndrome Disease MeSH Browser

Craniosynostosis Microcephaly with Chromosomal Breakage and Other Abnormalities Disease MeSH Browser

Craniosynostosis Syndrome, Autosomal Recessive Disease MeSH Browser

Craniosynostosis radial aplasia syndrome Disease MeSH Browser

Craniosynostosis with Anomalies of the Cranial Base and Digits Disease MeSH Browser

Craniosynostosis with Ectopia Lentis Disease MeSH Browser

Craniosynostosis with Fibular Aplasia Disease MeSH Browser

Craniosynostosis with Ocular Abnormalities and Hallucal Defects Disease MeSH Browser

Craniosynostosis, Adelaide Type Disease MeSH Browser

Craniosynostosis, Calcification of Basal Ganglia, and Facial Dysmorphism Disease MeSH Browser

Craniosynostosis, Philadelphia Type Disease MeSH Browser

Craniosynostosis, Type 2 Disease MeSH Browser

Craniosynostosis, anal anomalies, and porokeratosis Disease MeSH Browser

Craniosynostosis, sagittal, with Dandy-Walker malformation and hydrocephalus Disease MeSH Browser

Craniosynostosis-Mental Retardation Syndrome of Lin and Gettig Disease MeSH Browser

Craniotelencephalic dysplasia Disease MeSH Browser

Cutis Gyrata Syndrome of Beare And Stevenson Disease MeSH Browser

Fine-Lubinsky syndrome Disease MeSH Browser

Furlong syndrome Disease MeSH Browser

Genoa syndrome Disease MeSH Browser

Hordnes Engebretsen Knudtson syndrome Disease MeSH Browser

Hunter-McAlpine syndrome Disease MeSH Browser

Iida Kannari syndrome Disease MeSH Browser

Jackson-Weiss syndrome Disease MeSH Browser

Kleeblattschaedel syndrome Disease MeSH Browser

Lowry Maclean syndrome Disease MeSH Browser

Mehta Lewis Patton syndrome Disease MeSH Browser

Muenke Syndrome Disease MeSH Browser

Oculopalatoskeletal syndrome Disease MeSH Browser

Opitz trigonocephaly syndrome Disease MeSH Browser

Pfeiffer Tietze Welte syndrome Disease MeSH Browser

Piepkorn Karp Hickok syndrome Disease MeSH Browser

Plagiocephaly and X-linked mental retardation Disease MeSH Browser

Polycystic Kidney Disease, Potter Type I, with Microbrachycephaly, Hypertelorism, and Brachymelia Disease MeSH Browser

Scaphocephaly, Maxillary Retrusion, And Mental Retardation Disease MeSH Browser

Shprintzen Golberg craniosynostosis Disease MeSH Browser

Skeletal dysplasia, San Diego type Disease MeSH Browser

Spondyloepiphyseal Dysplasia With Coronal Craniosynostosis, Cataracts, Cleft Palate, And Mental Retardation Disease MeSH Browser

Trigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet Disease MeSH Browser

Trigonocephaly, Nonsyndromic Disease MeSH Browser