Mobius Syndrome [Moebiův syndrom]

topical
10
Terms

Möbiusův syndrom
Möbiův syndrom
syndrom kamenné tváře

 

Congenital Oculofacial Paralysis, Moebius
Congenital Ophthalmoplegia and Facial Paresis
Möbius Sequence
Moebius Congenital Oculofacial Paralysis
Moebius Sequence
Moebius Spectrum
Moebius Syndrome

Persistent link   https://www.medvik.cz/link/D020331
Definition

A syndrome of congenital facial paralysis, frequently associated with abducens palsy and other congenital abnormalities including lingual palsy, clubfeet, brachial disorders, cognitive deficits, and pectoral muscle defects. Pathologic findings are variable and include brain stem nuclear aplasia, facial nerve aplasia, and facial muscle aplasia, consistent with a multifactorial etiology. (Adams et al., Principles of Neurology, 6th ed, p1020)

DUI
D020331 MeSH Browser
CUI
M0008126
Previous indexing
Facial Paralysis (1966-1999)
History note
2000; use FACIAL PARALYSIS 1997-1999
Public note
2000: see FACIAL PARALYSIS 1997-1999

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification
CO
complications 2
DI
diagnosis 3
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy
EC
economics 1
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology
ET
etiology 2
GE
genetics 2
HI
history
IM
immunology
ME
metabolism
MI
microbiology
MO
mortality
NU
nursing 1
PS
parasitology
PA
pathology 3
PP
physiopathology 1
PC
prevention & control
PX
psychology 1
RT
radiotherapy
RH
rehabilitation 1
SU
surgery 2
TH
therapy 3
UR
urine
VE
veterinary
VI
virology

C Diseases
C07 Stomatognathic Diseases 117
C07.465 Mouth Diseases 428
C07.465.299 Facial Nerve Diseases 99
C07.465.299.250 Bell Palsy 49
C07.465.299.375 Facial Hemiatrophy 8
C07.465.299.500 Facial Nerve Injuries 29
C07.465.299.625 Facial Neuralgia 23
C07.465.299.750 Herpes Zoster Oticus 23
C07.465.299.800 Melkersson-Rosenthal Syndrome 20
C07.465.299.825 Mobius Syndrome 10
C10 Nervous System Diseases 1 878
C10.292 Cranial Nerve Diseases 60
C10.292.319 Facial Nerve Diseases 99
C10.292.319.250 Bell Palsy 49
C10.292.319.375 Facial Hemiatrophy 8
C10.292.319.500 Facial Nerve Injuries 29
C10.292.319.625 Facial Neuralgia 23
C10.292.319.750 Herpes Zoster Oticus 23
C10.292.319.800 Melkersson-Rosenthal Syndrome 20
C10.292.319.825 Mobius Syndrome 10
C10.292.562 Ocular Motility Disorders 101
C10.292.562.700 Oculomotor Nerve Diseases 20
C10.292.562.700.375 Congenital Cranial Dysinnervation Disorders
C10.292.562.700.375.500 Duane Retraction Syndrome 9
C10.292.562.700.375.750 Mobius Syndrome 10
C10.292.562.700.375.875 Septo-Optic Dysplasia 15
C11 Eye Diseases 1 489
C11.590 Ocular Motility Disorders 101
C11.590.436 Oculomotor Nerve Diseases 20
C11.590.436.400 Congenital Cranial Dysinnervation Disorders
C11.590.436.400.500 Duane Retraction Syndrome 9
C11.590.436.400.750 Mobius Syndrome 10
C11.590.436.400.875 Septo-Optic Dysplasia 15
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.131 Congenital Abnormalities 1 741
C16.131.077 Abnormalities, Multiple 330
C16.131.077.019 22q11 Deletion Syndrome 2
C16.131.077.065 Alagille Syndrome 19
C16.131.077.095 Angelman Syndrome 35
C16.131.077.121 Barth Syndrome 6
C16.131.077.130 Basal Cell Nevus Syndrome 33
C16.131.077.133 Beckwith-Wiedemann Syndrome 17
C16.131.077.137 Bloom Syndrome 11
C16.131.077.208 Branchio-Oto-Renal Syndrome 5
C16.131.077.229 Carney Complex 8
C16.131.077.245 Ciliopathies 9
C16.131.077.250 Cockayne Syndrome 4
C16.131.077.256 Costello Syndrome 3
C16.131.077.262 Cri-du-Chat Syndrome 11
C16.131.077.272 De Lange Syndrome 4
C16.131.077.299 Deaf-Blind Disorders 65
C16.131.077.313 Donohue Syndrome 1
C16.131.077.327 Down Syndrome 510
C16.131.077.350 Ectodermal Dysplasia 33
C16.131.077.371 Fraser Syndrome 2
C16.131.077.393 Gardner Syndrome 20
C16.131.077.401 Heterotaxy Syndrome 7
C16.131.077.410 Holoprosencephaly 8
C16.131.077.445 Incontinentia Pigmenti 19
C16.131.077.477 Isolated Noncompaction of the Ventricular Myocardium 11
C16.131.077.509 Laurence-Moon Syndrome 6
C16.131.077.525 LEOPARD Syndrome 11
C16.131.077.537 Loeys-Dietz Syndrome 7
C16.131.077.550 Marfan Syndrome 105
C16.131.077.578 Mobius Syndrome 10
C16.131.077.592 Monilethrix 1
C16.131.077.606 Nail-Patella Syndrome 8
C16.131.077.619 Netherton Syndrome 2
C16.131.077.633 Nevus, Sebaceous of Jadassohn 7
C16.131.077.662 Oculocerebrorenal Syndrome 9
C16.131.077.676 Orofaciodigital Syndromes 7
C16.131.077.690 Pallister-Hall Syndrome
C16.131.077.696 Pentalogy of Cantrell 1
C16.131.077.703 POEMS Syndrome 35
C16.131.077.717 Polycystic Kidney Diseases 82
C16.131.077.730 Prader-Willi Syndrome 92
C16.131.077.735 Prolidase Deficiency
C16.131.077.740 Proteus Syndrome 8
C16.131.077.745 Prune Belly Syndrome 3
C16.131.077.790 Rubella Syndrome, Congenital 20
C16.131.077.804 Rubinstein-Taybi Syndrome 12
C16.131.077.850 Short Rib-Polydactyly Syndrome 3
C16.131.077.855 Silver-Russell Syndrome 3
C16.131.077.860 Smith-Lemli-Opitz Syndrome 30
C16.131.077.879 Smith-Magenis Syndrome 2
C16.131.077.889 Sotos Syndrome 4
C16.131.077.899 Trichothiodystrophy Syndromes 1
C16.131.077.919 Trisomy 13 Syndrome 6
C16.131.077.929 Trisomy 18 Syndrome 5
C16.131.077.938 Waardenburg Syndrome 10
C16.131.077.941 Weill-Marchesani Syndrome 1
C16.131.077.944 Wolf-Hirschhorn Syndrome
C16.131.077.970 Zellweger Syndrome 10
C16.614 Infant, Newborn, Diseases 1 946
C16.614.042 Amniotic Band Syndrome 6
C16.614.053 Anemia, Neonatal 22
C16.614.092 Asphyxia Neonatorum 172
C16.614.131 Birth Injuries 158
C16.614.166 Colic 125
C16.614.183 Congenital Bone Marrow Failure Syndromes 2
C16.614.200 Congenital Hyperinsulinism 24
C16.614.213 Cystic Fibrosis 1 328
C16.614.258 Epilepsy, Benign Neonatal 13
C16.614.304 Erythroblastosis, Fetal 140
C16.614.378 Hernia, Umbilical 45
C16.614.438 Hydrophthalmos 9
C16.614.451 Hyperbilirubinemia, Neonatal 65
C16.614.465 Hyperostosis, Cortical, Congenital 13
C16.614.492 Ichthyosis 62
C16.614.521 Infant, Premature, Diseases 317
C16.614.580 Meconium Aspiration Syndrome 35
C16.614.595 Mobius Syndrome 10
C16.614.610 Neonatal Abstinence Syndrome 74
C16.614.627 Neonatal Sepsis 35
C16.614.643 Nystagmus, Congenital 8
C16.614.660 OEIS Complex
C16.614.677 Ophthalmia Neonatorum 12
C16.614.694 Persistent Fetal Circulation Syndrome 17
C16.614.760 Rothmund-Thomson Syndrome 7
C16.614.810 Sclerema Neonatorum 2
C16.614.815 Severe Combined Immunodeficiency 63
C16.614.868 Syphilis, Congenital 87
C16.614.890 Thanatophoric Dysplasia 7
C16.614.899 Thrombocytopenia, Neonatal Alloimmune 14
C16.614.909 Toxoplasmosis, Congenital 75
C16.614.940 Vitamin K Deficiency Bleeding 22
C16.614.947 Wolman Disease 15

Congenital facial diplegia Disease MeSH Browser

Moebius axonal neuropathy hypogonadism Disease MeSH Browser

Moebius syndrome 1 Disease MeSH Browser

Myopathy, congenital nonprogressive with Moebius and Robin sequences Disease MeSH Browser

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