نتایج جستجو برای: progressive hemifacial atrophy

تعداد نتایج: 149784  

 Wolfram Syndrome is a neurodegenerative autosomal recessive disorder. The occurrence of the disease should be suspected if non-autoimmune insulin-dependent diabetes occurs in an under-sixteen year old person having bilateral optic nerve atrophy. Diabetes insipidus (DI), neurosensory deafness, urinary track disorders, and nervous system complications are also seen in this disorder. The current ...

2013
V. Cervelli I. Bocchini C. Di Pasquali B. De Angelis G. Cervelli C. B. Curcio A. Orlandi M. G. Scioli E. Tati P. Delogu Pietro Gentile

The authors report their experience about the use of P.R.L. PLATELET RICH LIPOTRANSFERT method (platelet rich plasma mixed fat grafting) in 223 patients affected by soft tissue defects (ulcers, Romberg syndrome, Hemifacial atrophy, loss of substance, and signs of aging). This paper introduces the reader to PRP therapy and reviews the current literature on this emerging treatment modality, showi...

2012
Azize Esra Gürsoy Gülsen Babacan Yildiz Adam Mehmet Gülhan Mehmet Kolukisa

A 79-year-old female presented with five months history of progressive involuntary twitching movement on left face. Brain MR imaging revealed a heterogeneous T2 hyperintense lesion at left cerebellopontine angle. CT angiography showed a partially thrombosed saccular aneurysm of left PICA (posterior inferior cerebellar artery). The patient was treated with Botulinum toxin type A and almost total...

Journal: :acta medica iranica 0
h. ghaninejad k. balighi a. ehsani m. hoseini

kindler's syndrome is a rare entity of unknown cause characterized by acral blisters early in life followed by progressive diffuse poikiloderma and cutaneous atrophy. the inheritance pattern of this syndrome is not clear. we report four iranian siblings (three boys and one girl) with this syndrome, who were the result of a consanguineous marriage. in addition to the usual manifestations of the ...

2012
Yasser Salem

Spinal muscular atrophy (SMA) is a neuromuscular disorder characterized by degeneration of alpha motor neurons resulting in hypotonia, progressive muscular weakness and atrophy.30 Spinal muscular atrophy is one of the leading hereditary causes of infant mortality,31 it comprises the second most common fatal progressive diseases after cystic fibrosis.28 Spinal muscular atrophy is the most common...

Journal: :Proceedings of the Royal Society of Medicine 1924

Journal: :American Journal of Diseases of Children 1920

Journal: :The Boston Medical and Surgical Journal 1902

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