PANCOAST TUMOR PRESENTING WITH HORNER SYNDROME: A CASE REPORT
Malang Neurology Journal, 2023 Case Report: A 50-year-old man was referred to Dr. Moewardi General Hospital with history of right chest pain that radiate to the right back and hand for 2 months. His complaint did not improve with medication and physical therapy.
Raden Andi Ario Tedjo +4 more
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Plasma catecholamines, sweat electrolytes and physiological responses of exercised normal, partial anhidrotic and anhidrotic horses [PDF]
, 2009 Problem statement: Malaysia imports horses from temperate countries to develop equine sports in the country. Several of these horses developed partial and complete anhidrosis.
Abdullah, Rasedee +1 more
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Anhidrosis hemifrontal posquirúrgica
Revista Española de Anestesiología y Reanimación, 2014 El sindrome de Claude-Bernard-Horner, o paresia oculosimpatica, es un trastorno neurologico caracterizado por miosis, ptosis y anhidrosis. Puede ser el resultado de una lesion en cualquier punto a lo largo de la via simpatica originada en el hipotalamo (Anexo, ver material adicional online). Presentamos el caso de un paciente intervenido de un tumor de
Sevillano Torrado, Carlos +4 more
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Asymmetric anhidrosis in MSA [PDF]
Neurology, 2003 Thermodysregulation with loss of sweating is a common feature of dysautonomia in multiple system atrophy (MSA).1,2⇓ A 51-year-old man with MSA with …
C, Saft +4 more
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Painless self-mutilation − A case of hereditary sensory autonomic neuropathy type 4
Indian Journal of Paediatric Dermatology, 2022 Children with hereditary sensory and autonomic neuropathy (HSAN) Type IV present with loss of pain and temperature sensation and anhidrosis. They may sometimes exhibit aggressive and self-mutilating behavior. We present here the case of a 5-year-old male
Prateek Pathak +3 more
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55-year-old Woman with Headache, Vomiting, and Visual Disturbance [PDF]
, 2020 Case Presentation: A 55-year-old woman with a past medical history of hypertension, hyperlipidemia, and iron deficiency anemia presented to the emergency department with three days of headache, nausea, vomiting, and visual changes.
Murano, Tiffany +2 more
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Gene-Targeted Next Generation Sequencing Identifies PNPLA1 Mutations in Patients with a Phenotypic Spectrum of Autosomal Recessive Congenital Ichthyosis: The Impact of Consanguinity [PDF]
, 2017 Heritable forms of ichthyoses, also referred to as generalized Mendelian disorders of cornification, are phenotypically a highly heterogeneous group of conditions caused by mutations in a number of genes playing a role in keratinocyte differentiation ...
Abiri, Maryam +12 more
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Idiopathic Acquired Anhidrosis: Reversible Generalized Anhidrosis after Sunstroke
The Journal of Dermatology, 1999 AbstractIdiopathic acquired generalized anhidrosis is a very rare condition in which the pathogenesis is still unknown. Although varied findings have been reported, no consistent abnormal findings in sweat glands have been established by histological study or electronmicroscopic study.
T S, Chung, S H, Lee
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Congenital insensitivity to pain with anhidrosis
Journal of the Pakistan Medical AssociationCongenital Insensitivity to Pain with Anhidrosis (CIPA) is characterised by disruption of sensory neurons caused by genetic mutations in the Neurotrophic Tyrosine Kinase 1 (NTRK1) gene which leads to impaired pain sensation, accompanied by anhidrosis ...
Meher Ayyazuddin +4 more
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Meeting report: a hard look at the state of enamel research. [PDF]
, 2017 The Encouraging Novel Amelogenesis Models and Ex vivo cell Lines (ENAMEL) Development workshop was held on 23 June 2017 at the Bethesda headquarters of the National Institute of Dental and Craniofacial Research (NIDCR).
Bartlett, John D +13 more
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