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PROGRESSIVE FACIAL HEMIATROPHY, WITH SOME UNUSUAL SYMPTOMS [PDF]
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Hemifacial atrophy, including Parry-Romberg syndrome, is a rare, progressive disorder characterized by unilateral loss of facial soft tissue, with or without neurologic and/or ocular manifestations.
Al Farabi Lee Jaafar +2 more
doaj +1 more source
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. Clinically, the condition presents with contralateral
Yalcin, Ayse Destina +5 more
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Parry-romberg syndrome: difficulties of diagnosis and improvement of treatment
The article described a case of a rare disease – progressive facial hemiatrophy in a patient of the Neurological Department of Poltava Regional Clinical Hospital. We reviewed a literature on the problem, analyzed the etiological factors, pathogenesis and
Таряник, Катерина Анатоліївна +5 more
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Patient-induced progressive facial subcutaneous emphysema masquerading as odontogenic abscess
Facial subcutaneous emphysema (SE) is an uncommon sequelae of dental procedures and often attributed to the use of high-speed air-driven handpieces during surgical extractions, forcing air through fascial spaces.
Chang, Victor Ken On +3 more
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Localised Unilateral Facial Hemiatrophy
A very rare case of localized unilateral facial hemiatrophy is being presented ...
Gangopadhyay Asok +1 more
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Peripheral nervous system involvment in localized scleroderma with facial hemiatrophy
woman with facial hemiatrophy and ...
Tola M. R. +4 more
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Introduction: the progressive hemifacial atrophy or Parry-Romberg syndrome is a rare disease, of slow clinical evolution that generates atrophy of the soft tissues.
Redondo-Bermúdez César +4 more
doaj
Cortical silent period in a patient with focal epilepsy and Parry-Romberg syndrome
Progressive facial hemiatrophy (PFH), Parry-Romberg syndrome, is a rare disorder frequently associated with epilepsy. We describe a 28-year-old man who had PFH and partial epilepsy that was easily controlled with antiepileptic drugs.
Oguz, Y, Senol, U, Aktekin, B, Aydin, H
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Progressive Hemifacial Atrophy with Linear Scleroderma
We describe a 4-year-old girl with hemifacial atrophy. She had a linear white-colored sclerotic plaque on the right submandibular area of skin. Histologic findings of the lesion were consistent with a diagnosis of scleroderma.
Dervis, E, Emine Dervis, Emel Dervis
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