Results 31 to 40 of about 1,837 (197)

Facial Hemiatrophy [PDF]

The Journal of Nervous and Mental Disease, 1895
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openaire   +2 more sources

Marked hemiatrophy in carriers of Duchenne muscular dystrophy. [PDF]

, 2010
OBJECTIVE: To describe the clinical and molecular genetic findings in 2 carriers of Duchenne muscular dystrophy (DMD) who exhibited marked hemiatrophy. Duchenne muscular dystrophy is an X-linked disorder in which affected male patients harbor mutations ...
Holton, J.L., Storey, H., Lobrinus, J.A., Hanna, M.G., Rajakulendran, S., Kuntzer, T., Ashton, E.J., Leturcq, F., Abbs, S., Yau, S.C., Farmer, S., Thonney, F., Yousry, T., Dunand, M., McCauley, J.   +14 more
core   +3 more sources

FACIAL HEMIATROPHY [PDF]

The Journal of Nervous and Mental Disease, 1911
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openaire   +2 more sources

DYKE–DAVIDOFF–MASSON SYNDROME-A Rare Cause of Cerebral Hemiatrophy in a 17-Years-Old Ethiopian Patient: A Case Report [PDF]

, 2021
BACKGROUND: Dyke-Davidoff-Masson syndrome (DDMS) is a rare disease with unknown frequency, mainly presented with seizures, facial asymmetry, contralateral hemiparesis and mental retardation. Often, resulting from brain injury due to a multitude of causes,
Alemayehu Ayele, Biniyam, Zenebe Zewde, Yared   +1 more
core   +2 more sources

Proof of concept: Portable ultra-low-field magnetic resonance imaging for the diagnosis of epileptogenic brain pathologies. [PDF]

Epilepsia
Abstract Objective High‐field magnetic resonance imaging (MRI) is a standard in the diagnosis of epilepsy. However, high costs and technical barriers have limited adoption in low‐ and middle‐income countries. Even in high‐income nations, many individuals with epilepsy face delays in undergoing MRI.
Bauer T, Olbrich S, Groteklaes A, Lehnen NC, Zidan M, Lange A, Bisten J, Walger L, Faber J, Bruchhausen W, Vollmuth P, Herrlinger U, Radbruch A, Surges R, Sabir H, Rüber T.   +15 more
europepmc   +2 more sources

HEMIATROPHY OF THE TONGUE. [PDF]

The Lancet, 1900
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openaire   +1 more source

Cutis Marmorata Telangiectatica Congenita Associated with Hemiatrophy [PDF]

, 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.
Joseph M. Lam, Kin Fon Leong, Alexander K. C. Leung   +2 more
core   +1 more source

Você conhece esta síndrome? Do you know this syndrome?

Anais Brasileiros de Dermatologia, 2007
Trata-se de criança de oito anos, portadora de atrofia na hemiface direita, desde os seis anos. A ressonância magnética do encéfalo evidenciou espessamento cortical e formação de cistos.
Luciana Baptista Pereira, Rodrigo Santiago Gómez, Cláudia Márcia Resende Silva, Wandilza Fátima dos Santos   +3 more
doaj   +1 more source

Sclerosing diseases of the skin. [PDF]

J Dtsch Dermatol Ges
Summary Sclerosing skin diseases comprise a group of distinct dermatological conditions characterized by fibrotic changes that may severely impair patients’ quality of life. These conditions often present with cutaneous manifestations and, in some cases, may extend to extracutaneous tissues, potentially resulting in significant morbidity and mortality.
Kalantari Y, Meier K, Ghoreschi K, Kinberger M, Solimani F.   +4 more
europepmc   +2 more sources

Dyke-Davidoff-Masson Syndrome (DDMS) in Adult: A Rare Case in Rural Area

Aksona, 2023
Highlight: • Dyke-Davidoff-Masson syndrome (DDMS) is an uncommon neurological disease defined as cerebral hemiatrophy with a contralateral motor deficit, facial asymmetry, and seizures.
Indra Pramanasari
doaj   +1 more source