Results 111 to 120 of about 772 (152)

Parry-Romberg Syndrome and an Associated Complex Vascular Lesion Managed With Hybrid Strategies: A Case Report. [PDF]

Neurosurg Pract
Hagstrom R, Riina HA, Britz GW, Sharashidze V, Chung C, Weiss H, Spetzler RF, Nelson PK.   +7 more
europepmc   +1 more source

Parry-Romberg syndrome in Kuwait. Neurological manifestations in 2 children. [PDF]

Saudi Med J, 2019
Zakkiriah M, Al Khalaf MK, Al Mutairi MA, Al Enezi S.   +3 more
europepmc   +1 more source

Parry-Romberg Syndrome with Uhthoff's Phenomena: A Spectrum of Autoimmune Disease? [PDF]

Case Reports Immunol, 2019
Asanad S.
europepmc   +1 more source

Parry-Romberg syndrome in a patient with scleroderma. [PDF]

BMJ Case Rep, 2018
Kuah CY, Koleva E, Gan JJL, Iqbal T.
europepmc   +1 more source

Parry-Romberg Syndrome and Temporal Lobe Refractory Epilepsy: Case Report. [PDF]

J Epilepsy Res, 2019
Velandia-Martínez A, Ortega-Sanchez MA, Martínez-Perez SO, Peña I, Pradilla O, Gomez R, Martínez-Perez A.   +6 more
europepmc   +1 more source

Parry-Romberg syndrome

, 2017
openaire   +1 more source

[Parry-Romberg syndrome].

Neurologia (Barcelona, Spain), 1996
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A review of Parry-Romberg syndrome

Journal of the American Academy of Dermatology, 2012
Parry-Romberg syndrome, also known as progressive hemifacial atrophy, is a rare disorder characterized by unilateral facial atrophy affecting the skin, subcutaneous tissue, muscles, and sometimes extending to the osteocartilaginous structures. It has been associated with various systemic manifestations, particularly neurologic, ophthalmologic and ...
Nelly Rubeiz
exaly   +3 more sources

Parry Romberg syndrome

Indian Journal of Pediatrics, 2006
Parry-Romberg syndrome, which is also called progressive facial hemiatrophy, overlaps with a condition known as linear scleroderma “en coup de sabre”. It is a rare, acquired, neurocutaneous syndrome of unknown aetiology. The principle features are atrophy of the soft tissues, and sometimes the bone, on one half of the face or forehead without facial ...
Vandana Jain, Sheffali Gulati, Jain Vandana   +2 more
exaly   +3 more sources