Five Retained Soft Contact Lenses in the Upper Fornix: A Case Report in a Patient with Hemifacial Atrophy [PDF]
Plastic and Reconstructive Surgery, Global OpenSummary:. The displacement of a lost contact lens into the upper fornix is an uncommon occurrence. This case report presents a rare incidence wherein a patient diagnosed with hemifacial atrophy was found to have concealed five soft contact lenses within ...
Minghao Zhao, MD +3 more
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Autologous fat grafting in a case of Parry-Romberg syndrome: a case report [PDF]
Case Reports in Plastic Surgery & Hand SurgeryProgressive hemifacial atrophy, also known as Parry-Romberg syndrome (PRS), is an uncommon condition that causes slow and progressive unilateral soft-tissue atrophy of the face.
Bhakti Sarda +3 more
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Chronologic Presentation of a Severe Case of Progressive Hemifacial Atrophy (Parry-Romberg Syndrome) with the Loss of an Eye [PDF]
Case Reports in Otolaryngology, 2014 Progressive hemifacial atrophy, also known as Parry-Romberg syndrome, is a slowly advancing degenerative disease that mostly affects the cutaneous, subcutaneous fatty tissue, muscle tissue, and bone structures on one side of the face.
Mesut Kaya +3 more
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Prosthetic rehabilitation of an orbital defect for a patient with hemifacial atrophy [PDF]
The Journal of Indian Prosthodontic Society, 2016 Removal of an eye may be indicated in cases of congenital abnormality, severe trauma, or disease such as an infection, tumor, or malignancy. The disfigurement associated with a loss of an eye is often accompanied with physical problems, psychological ...
Sanath Shetty +3 more
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Unilateral Retinal Vasculitis as the Presenting Manifestation of Parry-Romberg Syndrome (Progressive Hemifacial Atrophy) [PDF]
Journal of Vitreoretinal Diseases, 2022 Aimee Szewka +2 more
exaly +2 more sources
Clinical Case ReportsParry‐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)
Sakib Abrar +4 more
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Dermatology Online Journal, 2013 We report the case of a 44-year-old woman with a one-year history of en coup de sabre morphea and progressive hemifacial atrophy with ipsilateral hemifacial neuralgia, migraine, and contralateral neurologic abnormalities. While rare, Parry-Romberg syndrome typically presents in the first or second decade of life; this patient's case is unusual in that ...
Vedvyas, Chetan, Urbanek, Richard W
openaire +5 more sources
Vascular Mechanisms in the Etiology of Hemifacial Microsomia: A Systematic Review of Epidemiological, Clinical, and Genetic Evidence. [PDF]
Birth Defects ResABSTRACT Background Hemifacial microsomia (HFM) is a congenital craniofacial malformation characterized by unilateral hypoplasia of structures derived from the first and second pharyngeal arches. Although the phenotype is well described, the underlying etiology remains incompletely understood.
Jacobs K +7 more
europepmc +2 more sources
Autologous adipose tissue transfer in progressive hemifacial atrophy: From simple volume to regenerative cell therapy [PDF]
JPRAS OpenAnne-Aurore Sankale, Matteo Scampa
exaly +2 more sources
Retinal vasculitis the first clue in the diagnosis of progressive hemifacial atrophy [PDF]
European Journal of Rheumatology, 2019 Atefeh Vafa +3 more
doaj +2 more sources