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Medial inferior pontine syndrome is a condition associated with a contralateral hemiplegia. [ citation needed ] "Medial inferior pontine syndrome" has been described as equivalent to Foville's syndrome .
Structures affected by the lesion are the dorsal pons (pontine tegmentum) which comprises paramedian pontine reticular formation (PPRF), nuclei of cranial nerves VI and VII, corticospinal tract, medial lemniscus, and the medial longitudinal fasciculus. There is involvement of the fifth to eighth cranial nerves, central sympathetic fibres ...
Marden–Walker syndrome; MASA syndrome; McLeod syndrome; Medial medullary syndrome; Medial pontine syndrome; Melkersson–Rosenthal syndrome; Menkes disease; Microcephaly albinism digital anomalies syndrome; Middle cerebral artery syndrome; Millard–Gubler syndrome; Mismatch repair cancer syndrome; Mitochondrial membrane protein-associated ...
Lateral pontine syndrome, also known as Marie-Foix syndrome or Marie-Foix-Alajouanine syndrome [1] is one of the brainstem stroke syndromes of the lateral aspect of the pons. A lateral pontine syndrome is a lesion which is similar to the lateral medullary syndrome , but because it occurs in the pons , it also involves the cranial nerve nuclei ...
Superior alternating hemiplegia or Weber's syndrome; Paramedian midbrain syndrome or Benedikt's syndrome; Claude's syndrome; Medial pontine syndrome or Middle alternating hemiplegia or Foville's syndrome; Lateral pontine syndrome or Marie-Foix syndrome; Medial medullary syndrome or Inferior alternating hemiplegia; Lateral medullary syndrome or ...
Middle alternating hemiplegia (also known as Foville Syndrome) typically constitutes weakness of the extremities accompanied by paralysis of the extraocular muscle, specifically lateral rectus, on the opposite side of the affected extremities, which indicates a lesion in the caudal and medial pons involving the abducens nerve root (controls movement of the eye) and corticospinal fibers ...
Millard–Gubler syndrome is named after two French physicians, Auguste Louis Jules Millard (1830–1915), who first identified the disorder in 1855, and Adolphe-Marie Gubler (1821–1879), who described the disease in a medical paper one year later.
In children, the most common cause is a stroke of the ventral pons. [9]Unlike persistent vegetative state, in which the upper portions of the brain are damaged and the lower portions are spared, locked-in syndrome is essentially the opposite, caused by damage to specific portions of the lower brain and brainstem, with no damage to the upper brain.