Acrocallosal Syndrome [syndrom corpus callosum]

topical
1
Terms

akrokalosální syndrom

 

Hallux Duplication, Postaxial Polydactyly, and Absence of Corpus Callosum

Persistent link   https://www.medvik.cz/link/D055673
Definition

Autosomal recessive syndrome characterized by hypogenesis or agenesis of CORPUS CALLOSUM. Clinical features include MENTAL RETARDATION; CRANIOFACIAL ABNORMALITIES; digital malformations, and growth retardation.

DUI
D055673 MeSH Browser
CUI
M0519414
Previous indexing
Congenital Abnormalities (1963-2008); Corpus Callosum (1963-2008)
History note
2009
Public note
2009

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification
CO
complications
DI
diagnosis
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology
ET
etiology
GE
genetics
HI
history
IM
immunology
ME
metabolism
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology 1
PP
physiopathology
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy
UR
urine
VE
veterinary
VI
virology

C Diseases
C10 Nervous System Diseases 1 878
C10.500 Nervous System Malformations 80
C10.500.034 Agenesis of Corpus Callosum 12
C10.500.034.500 Acrocallosal Syndrome 1
C10.500.034.687 Aicardi Syndrome
C10.500.034.875 Holoprosencephaly 8
C10.500.034.937 Septo-Optic Dysplasia 15
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.131 Congenital Abnormalities 1 741
C16.131.666 Nervous System Malformations 80
C16.131.666.034 Agenesis of Corpus Callosum 12
C16.131.666.034.500 Acrocallosal Syndrome 1
C16.131.666.034.687 Aicardi Syndrome
C16.131.666.034.875 Holoprosencephaly 8
C16.131.666.034.937 Septo-Optic Dysplasia 15

Acrocallosal syndrome, Schinzel type Disease MeSH Browser

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