Results 41 to 50 of about 3,677 (133)

Dyke-Davidoff-Masson syndrome: An endocrine perspective [PDF]

Romanian Medical Journal, 2020
Dyke-Davidoff-Masson syndrome (DDMS) represents a severe disease that is caused by brain anomalies of different mechanisms early in life during fetal period or within first years after birth.
Cristina Dumitrescu, Anda Dumitrascu, Corina Chirita, Eugenia Petrova, Nicoleta Dumitru, Adina Ghemigian, Mara Carsote, Dana Terzea, Ana Valea   +8 more
doaj   +1 more source

Cutis Marmorata Telangiectatica Congenita Associated with Hemiatrophy

Case Reports in Pediatrics, Volume 2020, Issue 1, 2020., 2020
Cutis marmorata telangiectatica congenita is characterized by the presence of a bluish‐purple reticulated cutaneous vascular network on the skin intermixed with telangiectasia and occasionally prominent veins at birth. Areas of the skin within the reticulated cutaneous vascular network may be normal, erythematous, atrophic, and, at times, ulcerated ...
Alexander K. C. Leung, Joseph M. Lam, Kin Fon Leong, Anselm Chi Wai Lee   +3 more
wiley   +1 more source

Dyke-Davidoff-Masson Syndrome as a rare congenital hemiatrophy: a case report: Dyke-Davidoff-Masson Syndrome

, 2021
Introduction: Dyke-Davidoff-Masson syndrome (DDMS) is a rare condition in childhood with very few cases reported in sub-Saharan Africa. Typically, the patient presents with facial asymmetry, seizures, and hemiparesis.
Nwako, Azubuike Benjamin, Nwako, Okechukwu Francis, Nwako, Magaret-Lorritta Chidimma, Nwolisa, Charles Emeka   +3 more
core   +1 more source

Dyke-Davidoff-Masson Syndrome: A Case Report

International Journal of Medical Students, 2022
Background: Dyke-Davidoff-Masson syndrome (DDMS) is a neurological syndrome characterized by the presence of convulsions, facial asymmetry due to palsy of the facial nerve (CN VII), contralateral hemiplegia, and reduced intellectual capacity. The Case:
Gaurav M. Urs, Hitesh R. Doddabele
doaj   +1 more source

Dyke-Davidoff-Masson syndrome: Two case reports [PDF]

, 2014
Dyke-Davidoff Masson sendromu nadir bir konjenital malformasyon olarak ilk kez 1933 yılında Dyke tarafından bildirilmiştir. Ana klinik bulguları; tek taraflı serebral atrofi, fasiyal asimetri, kontralateral hemiparezi ve epilepsidir.
Yavuz, Alpaslan, Göya, Cemil, Batur, Abdussamet, Bulut, Mehmet Deniz, Gülşen, İsmail, Bora, Aydın   +5 more
core   +1 more source

Dyke-Davidoff-Masson syndrome secondary to Sturge-Weber syndrome

Asian Journal of Surgery
Zhiqin Lin, Celin Guan, Tianqing Liu, Yuanxiang Lin   +3 more
doaj   +3 more sources

Dyke-Davidoff-Masson syndrome presenting with recurrent seizures [PDF]

Romanian Journal of Neurology, 2016
Dyke-Davidoff-Masson syndrome (DDMS) is cerebral hemiatrophy occurring following brain insult resulting from infarct, trauma or infection in utero or soon after birth.
M. Rajaguru, V. Umamaheswara Reddy, Amit Agrawal, V. Ganesh, Anil Tadikonda   +4 more
doaj   +1 more source

A case of Dyke-Davidoff-Masson syndrome

, 2012
Dyke-Davidoff-Masson syndrome is a condition characterized by seizures, facial asymmetry, contralateral hemiplegia or hemiparesis and mental retardation. The clinical findings may be of variable degree according to the extent of brain injury.
Ali Yikilmaz, GÜMÜŞ, HAKAN, Yikilmaz, Ali, Soylu, Pembe, Poyrazoglu, Hatice Gamze, Hakan Gumus, Huseyin Per, Hatice Poyrazoglu, Mehmet Canpolat, Kumandas, Sefer, PER, HÜSEYİN, CANPOLAT, MEHMET, Pembe Soylu, Sefer Kumandas   +13 more
core   +1 more source

Neurodevelopmental influences in psychosis: a case of left cerebral hemiatrophy and schizoaffective disorder

Psychiatry and Clinical Psychopharmacology, 2021
Cerebral hemiatrophy (or Dyke-Davidoff-Masson Syndrome) is a neurodevelopmental disorder characterized by atrophy or hypoplasia of one cerebral hemisphere accompanied by ipsilateral calvarial changes.
Asli Demirtas Tatlidede, Ayse Destina Yalcin, Tugba Guven Canpolat   +2 more
doaj   +1 more source

Dyke-Davidoff-Masson syndrome: case report of fetal unilateral ventriculomegaly and hypoplastic left middle cerebral artery [PDF]

, 2013
Prenatal ultrasonographic detection of unilateral cerebral ventriculomegaly arises suspicion of pathological condition related to cerebrospinal fluid flow obstruction or cerebral parenchimal pathology.
PICCIONE, Maria, GIUFFRE, Mario, CORSELLO, Giovanni, PIRO, Ettore, Marrone, G   +4 more
core   +1 more source