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We reviewed the literature on published cases of progressive facial hemiatrophy (Parry-Romberg syndrome) to identify possible pathophysiological mechanisms of the ...
Goadsby, Peter J. +5 more
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ABSTRACT Parry‐Romberg Syndrome (PRS) is a rare disorder characterized by progressive unilateral facial atrophy, traditionally viewed as a localized scleroderma variant. Its rare coexistence with systemic lupus erythematosus (SLE) and autoimmune thyroiditis (AIT) suggests a broader inflammatory etiology, challenging the notion of PRS as a purely ...
Sakib Abrar +4 more
wiley +1 more source
Trigeminal neuralgia, migraine and sympathetic hyperactivity in a patient with Parry–Romberg syndrome [PDF]
Parry–Romberg syndrome is a rare disorder of unknown aetiology that involves slowly progressive but self-limited wasting of subcutaneous tissues on one side of the face, usually in the distribution of a branch of the trigeminal nerve.
Drummond, P.D., Finch, P.M., Hassard, S.
core
Dyke‐Davidoff‐Masson Syndrome: A Case of Unilateral Cerebral Atrophy and Seizure Disorder
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.
Wasfa Shafiq +7 more
wiley +1 more source
:e313-6. Parry Romberg Syndrome: A rare entity Journal section: Oral Medicine and Pathology Publication Types: Case Report Parry Romberg Syndrome with localized scleroderma: a case report [PDF]
Parry Romberg syndrome(PRS) is a rare acquired poorly understood neurocutaneous syndrome of unknown etiology characterized by slow progressive atrophic changes commonly affecting one half of the face. The exact incidence and etiology towards the syndrome
Mubeen Khan +6 more
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Parry Romberg Syndrome. An unusual case with dental features.
Parry-Romberg syndrome, also known as progressive hemi facial atrophy has been described as having clinical overlap with Morphea en coup de sabre or linear scleroderma.
Cj Bates, Hamed Safaei*, Tk Mittal
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Coexistence of Localized and Systemic Juvenile Scleroderma: A Case Report and Review of Literature
ABSTRACT Juvenile scleroderma (JS) is a rare chronic connective tissue disorder characterized by progressive fibrosis of the skin and soft tissues with/without internal organ involvements. Scleroderma manifests itself in both systemic (SSc) and localized (LS) forms.
Aye Miremarati +4 more
wiley +1 more source
Lipostructure in Parry-Romberg Disease
Parry-Romberg syndrome is a disease characterized by progressive hemifacial atrophy. Multiple surgical procedures have been used to improve the facial volume and contours of patients with this disease, including alloplastic, silicone, or collagen ...
TERENZI, VALENTINA +5 more
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Unveiling Parry-Romberg Syndrome With Native Demyelinating Etiology as the Underlying Cause
Parry-Romberg Syndrome (PRS) is an atypical condition characterized by hemiatrophy of the face. Despite its rarity, the precise pathophysiological processes underlying its etiology remain elusive.
Kaveh Bahram +4 more
doaj +1 more source
Progressive hemifacial atrophy (Parry-Romberg Syndrome)
Progressive hemifacial atrophy, also known as Parry-Romberg Syndrome, is an uncommon degenerative and poorly understood condition. It is characterized by a slow and progressive atrophy affecting one side of the face.
S A Deshingkar +3 more
doaj +1 more source

