Search on: HORNER SYNDROME 
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Descriptor English:   Horner Syndrome 
Descriptor Spanish:   Síndrome de Horner 
Descriptor Portuguese:   Síndrome de Horner 
Synonyms English:   Bernard Syndrome
Horner's Syndrome
Miosis, Innervational Defect
Oculosympathetic Syndrome  
Tree Number:   C10.177.350
C10.597.690.362.500
C11.710.528.500
C23.888.592.708.362.500
Definition English:   A syndrome associated with defective sympathetic innervation to one side of the face, including the eye. Clinical features include MIOSIS; mild BLEPHAROPTOSIS; and hemifacial ANHIDROSIS (decreased sweating)(see HYPOHIDROSIS). Lesions of the BRAIN STEM; cervical SPINAL CORD; first thoracic nerve root; apex of the LUNG; CAROTID ARTERY; CAVERNOUS SINUS; and apex of the ORBIT may cause this condition. (From Miller et al., Clinical Neuro-Ophthalmology, 4th ed, pp500-11) 
History Note English:   2000(1966) 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications CN congenital
DI diagnosis 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
PP physiopathology PC prevention & control
PX psychology RA radiography
RI radionuclide imaging RT radiotherapy
RH rehabilitation SU surgery
TH therapy US ultrasonography
UR urine VE veterinary
VI virology  
Record Number:   28095 
Unique Identifier:   D006732 

Occurrence in VHL:
 

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