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Hemiatrofia facial progressiva (doença de Parry-Romberg): relato de dois casos associados a trigeminalgia e câimbras Progressive facial hemiatrophy (Parry-Romberg disease): report of two cases associated with trigeminal neuralgia and cramps [PDF]

Arquivos de Neuro-Psiquiatria, 1997
Os autores relatam dois casos de hemiatrofia facial progressiva (HFP), ambos do sexo feminino, associados à hiperexcitabilidade neuromuscular, representada por dores neurálgicas e espasmos musculares (câimbras) numa hemiface.
José Correia de Farias Brito, Maurus Marques de Almeida Holanda, Glerystane Holanda, José Alberto Gonçalves da Silva   +3 more
doaj   +2 more sources

Idiopathic acquired progressive left facial hemiatrophy (Parry-Romberg syndrome) in a 21-year-old man in semi-urban, south-west Nigeria [PDF]

South African Family Practice, 2011
Idiopathic progressive hemifacial atrophy, or Parry-Romberg syndrome, is a rare entity, seldom described in medical texts. Though first described in 1825, as yet there are no clear-cut diagnostic criteria. It is of interest mainly because of the numerous
F.A. Imarhiagbe, A.O. Adeoti
doaj   +7 more sources

Adult Presentation of Dyke-Davidoff-Masson Syndrome: A Case Report [PDF]

Case Reports in Neurology, 2016
Dyke-Davidoff-Masson syndrome (DDMS) is a rare disease which is clinically characterized by hemiparesis, seizures, facial asymmetry, and mental retardation.
Ujjawal Roy, Ajay Panwar, Adreesh Mukherjee, Debsadhan Biswas   +3 more
doaj   +2 more sources

A case of progressive facial hemiatrophy. [PDF]

Japanese Journal of Oral & Maxillofacial Surgery, 1991
There are very few papers showing clear dental findings in progressive facial hemiatrophy. A case of progressive facial hemiatrophy of the right side with a number of dental abnormalities in a 10-year-old girl is reported.There were no systemic abnormalities.
NISHIKATA, Satoshi, HIRANO, Masayasu, HANDA, Yukio, NAKAMURA, Eiji, KUDO, Akihiro, AHMED, Mohiuddin, DOIGAMI, Teruo, MIKOYA, Tadashi, FUJIWARA, Toshikatsu, MATSUDA, Akemi, INOUE, Nobuo, KAWAMURA, Masaaki   +11 more
openaire   +3 more sources

Progressive facial hemiatrophy with associated osseous lesions. [PDF]

Medicina oral, patologia oral y cirugia bucal, 2007
Progressive facial hemiatrophy (PFH) is a rare condition characterized by the slow, progressive appearance of a unilateral facial atrophy that affects the skin, subcutaneous tissue, muscle and bone. We report the case of a 60-year-old female patient whose cutaneous symptoms commenced in 1987 in the form of a purplish erythema on the left side of her ...
Gómez Diez, Santiago, Gallego López, Lorena, López Escobar, María, Junquera Gutiérrez, Luis, Pérez Oliva, Narciso   +4 more
openaire   +6 more sources

Dyke-Davidoff-Masson Syndrome: A Case of Unilateral Cerebral Atrophy and Seizure Disorder. [PDF]

Clin Case Rep
ABSTRACT Dyke‐Davidoff‐Masson syndrome (DDMS) is an infrequently occurring neurological entity characterized by cerebral hemiatrophy and a collection of cognitive, motor and seizure‐related symptoms. We describe the case of an 18‐year‐old male with a long‐standing history of generalized tonic–clonic seizures following a significant fall at the age of 4.
Shafiq W, Majeed HM, Farooqi HH, Khaliq MW, Chohan DA, Mushtaq A, Gohar A, Ahmad MH.   +7 more
europepmc   +2 more sources

Połowiczy zanik twarzy bez zmian w ośrodkowym układzie nerwowym i twardzina en coup de sabre z guzem zewnątrzmózgowym – opis przypadków [PDF]

Przegląd Dermatologiczny, 2011
Introduction. Progressive facial hemiatrophy (Parry-Romberg syndrome)is a relatively rare disease of unclear aetiology. Some authorspostulate its relation with linear scleroderma.Objective.
Ligia Brzezińska-Wcisło, Anna Lis-Święty, Beata Bergler-Czop   +2 more
doaj   +1 more source

Dyke-Davidoff-Masson Syndrome in a Female Adult: A Rare Case of Progressive Hemiparesis, Epilepsy, and Cerebral Hemiatrophy. [PDF]

Clin Case Rep
ABSTRACT Consideration of Dyke‐Davidoff‐Masson syndrome (DDMS) in patients with epilepsy, hemiparesis, and cognitive impairment should be taken into account. MRI plays a key role in diagnosing this rare disorder by recognizing cerebral hemiatrophy with compensatory skull and sinus hypertrophy.
La QD, Baloch A, Ayub M, Ahmed S, Lue E.
europepmc   +2 more sources

Case Report of Rasmussen's Encephalitis With a Decade of Refractory Epilepsy and Hemispheric Atrophy. [PDF]

Clin Case Rep
ABSTRACT Rasmussen's encephalitis (RE) is a rare, chronic inflammatory neurological disorder affecting one cerebral hemisphere and presenting with drug‐resistant epilepsy, progressive hemiparesis, and cognitive decline. This case report describes the clinical course and management of a 21‐year‐old patient with refractory epilepsy and progressive ...
Al-Badri S, Duhan A, Al-Taie RH, Abbas AH, Abdulgadir A, Khalil I, Bacha Z, Al-Gizey N.   +7 more
europepmc   +2 more sources

High-Frequency Ultrasound Assessment of Skin Thickness Following Lipofilling in Facial Sclerosing Dermatoses: A Case Series. [PDF]

J Cosmet Dermatol
Journal of Cosmetic Dermatology, Volume 24, Issue 5, May 2025.
Gomez-Martinez S, Fuertes I, Ferrer Fuertes A, Gonzalez FJC, Martí Pagés C, Lledó-Ibáñez GM, Espinosa G, Quintana-Codina M, Iglesias Sancho M, Cembrano MD, Bosch-Amate X, Mascaró JM, Giavedoni P.   +12 more
europepmc   +2 more sources