Hemifacial atrophy
A rare disorder of unknown etiology, which is characterized by slowly progressive, unilateral facial atrophy of the skin, soft tissue, muscles, and underlying bony structures. Neurological, ocular, and oral symptoms are also often seen, including migraines, trigeminal neuralgia, enophthalmos, and dental and gingival abnormalities.
Disease Alternative Name
Recent Cases of Hemifacial atrophy
Browse recently discussed Hemifacial atrophy cases by specialists
Dear Dr.Saket Fat gives EXTRAORDINARY results in Romberg's .But there are equal chances of fat absorption which is earlier and fast as compared to n person .Explain well to patient that she may require more than one sesdoon and every time o...
1 Like
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Top Hemifacial atrophy Doctors on Curofy
Top doctors who continously share their opinions on Hemifacial atrophy
Jagadguru Jayadeva Murugarajendra Medical College
Retired Professor and Head Pediatrics
Jagadguru Jayadeva Murugarajendra Medical College
md,frcpch(uk),ficpcc(London),masp(usa),phd, fams ,fimsa.
AADESH MEDICAL COLLEGE
Associate Professor HEAD OF UNIT PAEDIATRIC
Dr SN Medical College Jodhpur
MD PAEDS
GH
Insurance Medical Officer
Madurai Medical College
MBBS
Vivekananda Polyclinic And Institute Of Medical Sciences
Junior Resident
Vivekananda Polyclinic And Institute of Medical Sciences
DNB OPHTHALMOLOGY
New Phc
Ayush Pharmashist
Kanpur Para Medical Institute
d.pharma
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30 years non diabetic male presented with feet deformities, trophic ulcer and osteomyelitis of the right foot gradually increasing since 3 years. He consulted many doctors but was not diagnosed for 3 years. Health system delay for diagnosis could've been avoided. What a price to pay for a delayed diagnosis! What is your diagnosis? Awareness and knowledge will minimise health system delay. Thank you.
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Tibial aplasia and prosthetic Leg restoration. *Chief Complaints* Due to congenital anomalies she walks with abnormal gait patterns. *History* When she was born 28 years ago with such congenital anomalies. Her parents never thought that their 5th girl child would be the same as others 4 . But she had different problems with tibial aplasia and others 4 having complex syndactyly in both hands. Same as their father having complex syndactyly. *Vitals* Unable to perform activities of daily living. *Physical Examination* Problem with walking and gripping and grasping. *Management* 28 years old girl looking for Prosthetics management for tibial aplasia. Our team takes measurements and casting for Prosthetic Leg restoration. Now she walks comfortably with a new prosthetic Leg.
Dr. Narendra Kumar1 Like2 Answers - Login to View the image
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