Results 71 to 80 of about 2,367 (191)
Hemimegalencephaly with intractable epilepsy: A case report [PDF]
, 2017 Isolated Hemimegalencephaly (iHME) is a rare form of congenital malformation of cortical development.It is characterized by enlargement of all or part of one cerebral hemisphere.
Raghib, Muhammad Faraz +2 more
core
Association between hemimegalencephaly and tuberous sclerosis in patients with epilepsy
, 2018 Introdução: A hemimegalencefalia é uma rara malformação cerebral que envolve o crescimento anormalmente maior de um hemisfério cerebral. Clinicamente, observase macrocefalia, retardo mental, hemiparesia contralateral, hemianopsia e epilepsia intratável ...
Coutinho, Larissa Cristina de Queiroga Mendonça
core +1 more source
South African Journal of Radiology, 2015 Congenital infiltrating lipomatosis of the face (CILF) is a rare disorder in which overgrowth of fatty tissue with infiltration of underlying structures leads to craniofacial deformities and asymmetry.
Eric Gous +2 more
doaj +1 more source
Hypomelanosis of Ito with hemimegalencephaly
Dermatology Online Journal, 2009 Hypomelanosis of Ito is a neurocutaneous syndrome characterized by hypopigmented lesions occurring in streaks and whorls located on the trunk, head or extremities. The associated neurological manifestations include mental retardation, seizures, language disabilities and motor system dysfunction. Hemihypertrophy has also been described in this syndrome.
Sharma, Suvasini +3 more
openaire +4 more sources
European Journal of Neurology, Volume 33, Issue 2, February 2026.Hereditary hemorrhagic telangiectasia (HHT) and several HHT‐like syndromes, including Wyburn–Mason, Cobb, Klippel–Trénaunay, Parkes Weber, neurofibromatosis type 1, PHACE(S), capillary malformation–AVM (CM‐AVM), Juvenile polyposis/HHT overlap, HHT type 5, PTEN hamartoma tumor syndrome, and blue rubber bleb nevus syndrome, share overlapping ...
Matteo Palermo, Carmelo Lucio Sturiale
wiley +1 more source
Hemimegalencephaly in a Patient With a Neurocutaneous Syndrome
, 2008 A 5-year-old girl with a history of hypomelanosis of Ito and intractable epilepsy was evaluated for possible resective surgery. Magnetic resonance imaging showed an enlarged right hemisphere, whereas electrographic seizures were arising from the right ...
Chapman, Kevin, Cardenas, Javier F.
core +1 more source
Ohtahara syndrome and IVF: A case report [PDF]
Acta Medica Iranica, 2000 Ohtahara syndrome or ealy infantile epileptic encephalopathy is a rare cause of epileptic seizures during infancy and represents the earliest type of age related symptomatic generalized epilepsies.
Ashrafi NR
doaj +1 more source
, 2013 Learning objectives: Description through two cases, one type of neuronal migration anomaly that occurs during cortical...
openaire +2 more sources
, 2015 We report on the youngest infant treated with modified functional hemispherectomy at the age of 5 months for Ohtahara syndrome and hemimegalencephaly as underlying pathology, and we depict the favorable outcome regarding seizure control and psychomotor ...
Alaywan, Moussa +5 more
core +1 more source