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 DeCS Categories

C05 Musculoskeletal Diseases .
C05.116 Bone Diseases .
C05.116.099 Bone Diseases, Developmental .
C05.116.099.708 Osteochondrodysplasias .
C05.116.099.708.025 Acquired Hyperostosis Syndrome .
C10 Nervous System Diseases .
C10.177 Autonomic Nervous System Diseases .
C10.177.350 Horner Syndrome .
C10.597 Neurologic Manifestations .
C10.597.690 Pupil Disorders .
C10.597.690.362 Miosis .
C10.597.690.362.500 Horner Syndrome .
C11 Eye Diseases .
C11.710 Pupil Disorders .
C11.710.528 Miosis .
C11.710.528.500 Horner Syndrome .
C23 Pathological Conditions, Signs and Symptoms .
C23.888 Signs and Symptoms .
C23.888.592 Neurologic Manifestations .
C23.888.592.708 Pupil Disorders .
C23.888.592.708.362 Miosis .
C23.888.592.708.362.500 Horner Syndrome .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Horner Syndrome .
Bernard's Syndrome .
Claude Bernard-Horner Syndrome .
Horner Syndrome, Acquired .
Horner Syndrome, Central .
Horner's Syndrome, Pupil .
Ophthalmoplegia, Sympathetic Ocular .
Ptosis Sympathetic .
Sympathetic Ocular-Ophthalmoplegia .
Acquired Horner Syndrome .
Bernard Syndromes .
Bernards Syndrome .
Central Horner Syndrome .
Claude Bernard Horner Syndrome .
Horner Syndrome, Pupil .
Horners Syndrome .
Horners Syndrome, Pupil .
Ocular Ophthalmoplegia, Sympathetic .
Ocular Ophthalmoplegias, Sympathetic .
Ocular-Ophthalmoplegia, Sympathetic .
Ocular-Ophthalmoplegias, Sympathetic .
Oculosympathetic Syndromes .
Ophthalmoplegias, Sympathetic Ocular .
Pupil Horner's Syndrome .
Sympathetic Ocular Ophthalmoplegia .
Sympathetic Ocular Ophthalmoplegias .
Sympathetic Ocular-Ophthalmoplegias .
Syndrome, Acquired Horner .
Syndrome, Bernard .
Syndrome, Bernard's .
Syndrome, Central Horner .
Syndrome, Claude Bernard-Horner .
Syndrome, Horner .
Syndrome, Horner's .
Syndrome, Oculosympathetic .
Syndrome, Pupil Horner's .
Syndromes, Bernard .
Syndromes, Oculosympathetic .
Bernard Syndrome .
Horner's Syndrome .
Miosis, Innervational Defect .
Oculosympathetic Syndrome .
BERNARD'S SYNDROME .
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) .
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Acquired Hyperostosis Syndrome .
Synovitis, Acne, Pustlosis, Hyperostosis, and Osteomyelitis .
Acquired Hyperostosis Syndromes .
Hyperostosis Syndrome, Acquired .
Hyperostosis Syndromes, Acquired .
SAPHO Syndromes .
Syndrome, Acquired Hyperostosis .
Syndrome, SAPHO .
Syndromes, Acquired Hyperostosis .
Syndromes, SAPHO .
SAPHO Syndrome .
Syndrome consisting of SYNOVITIS; ACNE CONGLOBATA; PALMOPLANTAR PUSTULOSIS; HYPEROSTOSIS; and OSTEITIS. The most common site of the disease is the upper anterior chest wall, characterized by predominantly osteosclerotic lesions, hyperostosis, and arthritis of the adjacent joints. The association of sterile inflammatory bone lesions and neutrophilic skin eruptions is indicative of this syndrome. .
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