Unstable Gait: Causes & Reasons

Possible Causes for Unstable Gait

His gait was unstable and he could not walk in tandem. His behavior was disinhibited and he expressed paranoid and delusional thoughts. [the-rheumatologist.org]

Autosomal Recessive Spinocerebellar Ataxia Type 17

Gait ataxia is characterized by unstable walk and standing, which slowly progresses with the appearance of some of the other symptoms, such as abnormal hand movements, involuntary [encyclopedia.com]

SCA10 ataxia is caused by an unstable protein repeat on chromosome 22. [encyclopedia.com]

Dystonia (spasticity or involuntary and repetitive movements) or gait ataxia is usually the initial symptom in children. [encyclopedia.com]

Autosomal Recessive Spinocerebellar Ataxia

His gait became progressively unstable from childhood, and started to interfere with his daily activities after the age of 45. [jmg.bmj.com]

Congenital Disorder of Glycosylation Type 2A

On examination, he had severe mental retardation with no speech and an unstable gait. [jmg.bmj.com]

Non-Hodgkin Lymphoma

You are here Home Types of Cancer Lymphoma - Non-Hodgkin Lymphoma - Non-Hodgkin This is Cancer.Net’s Guide to Lymphoma - Non-Hodgkin. Use the menu below to choose the Introduction section to get started. Or, you can choose another section to learn more about a specific question you have. Each guide is[…] [cancer.net]

Lyme Neuroborreliosis

A positive antibody response may lead to more confusion than clarification. Borrelia bacteria can be transmitted to humans through tick bites and give rise to Lyme neuroborreliosis. Disease manifestation varies in terms of symptoms and time course. Most patients experience subacute onset of neurological symptoms[…] [tidsskriftet.no]

Lyme Disease

Practice Essentials Lyme disease, the most common vector-borne illness in the United States, is a multisystem illness usually caused by infection with the spirochete Borrelia burgdorferi (see the image below) and the body's immune response to the infection. [1] The disease is transmitted to humans via tick bites,[…] [emedicine.medscape.com]

X-linked Distal Spinal Muscular Atrophy Type 3

Homepage Rare diseases Search Search for a rare disease X-linked distal spinal muscular atrophy type 3 Disease definition X-linked distal spinal muscular atrophy type 3 is a rare distal hereditary motor neuropathy characterized by slowly progressive atrophy and weakness of distal muscles of hands and feet with[…] [orpha.net]

Limb-Girdle Muscular Dystrophy Type 2C

BACKGROUND: Limb-girdle muscular dystrophy type 2C (LGMD2C) is an autosomal recessive muscle dystrophy that resembles Duchenne muscular dystrophy (DMD). Although DMD is known to affect one in every 3500 males regardless of race, a widespread founder mutation causing LGMD2C has been described in North Africa.[…] [ncbi.nlm.nih.gov]

Huntington Disease-Like Type 1

Home / Genetic Testing / Test Catalogue / By Test (A-Z) / Huntington disease-like 1 (HDL1, detection of expansion on PRNP gene) < Back to results Huntington disease-like 1 (HDL1, detection of expansion on PRNP gene) PRNP Request Now Methodology Fragment analysis and RP-PCR Specimen Requirements Descriptive[…] [cgcgenetics.com]

Huntington Disease-Like Type 3

WHO-ICD-10 version:2010 Diseases of the nervous system Systemic atrophies primarily affecting the central nervous system Mode of Inheritance Autosomal Recessive Gene Map Locus Huntington disease-like (HDL) syndromes are conditions that resemble Huntington disease, but are not caused by the same mutant[…] [cags.org.ae]

Aromatic L-Amino Acid Decarboxylase Deficiency

AADC stands for Aromatic L-Amino Acid Decarboxylase Deficiency This definition appears somewhat frequently and is found in the following Acronym Finder categories: Science, medicine, engineering, etc. See other definitions of AADC Samples in periodicals archive: The diseases identified to date include: tyrosine[…] [acronymfinder.com]

Malignant Atrophic Papulosis

Type your tag names separated by a space and hit enter Abstract The authors report a case of Degos' malignant atrophic papulosis (MAP) with typical skin lesions from a clinical and histological standpoint. They stress in particular the ultrastructural study of skin biopsies which revealed numerous[…] [unboundmedicine.com]

Thrombotic Thrombocytopenic Purpura

Thrombotic thrombocytopenic purpura is a disorder of microvascular thrombosis characterized by a sudden onset of hemolytic anemia, thrombocytopenia, and neurologic abnormalities that may be life-threatening without immediate treatment. Impaired regulation of von Willebrand factor (vWF) activity due to deficiency of[…] [symptoma.com]

Creutzfeldt Jakob Disease

News A urine test for Creutzfeldt-Jakob Disease may be possible Contact the Press Office MRC Talks podcast Network magazine Insight blog Back to listing 3 Oct 2016 Researchers at the MRC Prion Unit at UCL have found that it may be possible to determine whether or not a person has sporadic Creutzfeldt-Jakob[…] [mrc.ukri.org]

Autosomal Recessive Spastic Paraplegia Type 56

Chad A. Noggle, Raymond S. Dean, Arthur MacNeill Horton Springer Publishing Company, 2012 - 804 من الصفحات I am pleased to include this text in my library, and I am confident that it will serve as an excellent resource for years to come."-- PsycCRITIQUES This book serves as an A-Z reference that addresses the[…] [books.google.com]

Infantile Neuroaxonal Dystrophy

From Wikidata Jump to navigation Jump to search No description defined infantile neuroaxonal dystrophy INAD PLAN Seitelberger disease Hunter-Carpenter-McDonald syndrome Infantile neuroaxonal dystrophy Phospholipase A2-associated neurodegeneration INAD1 edit English Infantile neuroaxonal dystrophy No description[…] [wikidata.org]

Advanced Parkinson Disease

Plague

MSD Manual Professional Version The trusted provider of medical information since 1899 VIEW CONSUMER VERSION HOME MEDICAL TOPICS Common Health Topics Cardiovascular Disorders Clinical Pharmacology Critical Care Medicine Dental Disorders Dermatologic Disorders Ear, Nose, and Throat Disorders Endocrine and Metabolic[…] [msdmanuals.com]

Charcot-Marie-Tooth Disease Type 2T

Title Other Names: Autosomal dominant hereditary motor and sensory neuropathy type 2 with giant axons; CMT2 with giant axons; HMSN2 with giant axons Categories: This disease is grouped under: The following summary is from Orphanet, a European reference portal for information on rare diseases and orphan drugs.[…] [rarediseases.info.nih.gov]

Autosomal Recessive Mental Retardation Type 38

REFERENCIAS BIBLIOGRÁFICAS 1. Real Academia Española. Inteligencia. Madrid: Real Academia Española; 2019. (Citado el 30 de marzo de 2020) Disponible en: http://lema.rae.es/drae2001/srv/search?id=2qlbggjrBDXX2HVuWUL7 [ Links ] 2. Sternberg RJ. Intelligence. Dialogues Clin Neurosci. 2012;14(1):19-27. [ Links ] 3. Plomin R, von[…] [scielo.org.pe]

Combined Oxidative Phosphorylation Deficiency 15

< Back to results Combined oxidative phosphorylation deficiency type 15 (sequence analysis of MTFMT gene) MTFMT Request Now Methodology Sanger sequencing Specimen Requirements Descriptive Volume / Concentration 1 Container Transport temperature Sample viability (days) 2 DNA ≥ 100 µL [50 ng/µL] Eppendorf[…] [cgcgenetics.com]

Distal Hereditary Motor Neuropathy Type 5B

Nome malattia codice esenzione malattia di riferimento NEUROFIBROMATOSI-SINDROME DI NOONAN RBG010 NEUROFIBROMATOSI NEUROLIPOMATOSI RC0090 MALATTIA DI DERCUM NEUROMIOTONIA ACQUISITA RN1490 SINDROME DI ISAACS NEUROPATIA - ATASSIA - RETINITE PIGMENTOSA RCG078 DIFETTI CONGENITI DELLA FOSFORILAZIONE OSSIDATIVA[…] [malattierare.regione.veneto.it]

X-Linked Syndromic Mental Retardation Type Chudley-Schwartz

Disease Ontology : 12 A syndromic X-linked intellectual disability characterized by moderate intellectual disability, seizures, dysmorphic facial features and in some older patients slowly progressive unsteady gait and progressive weakness that has material basis in variation in the chromosomal region Xq21.33-q23.[…] [malacards.org]

Limb-Girdle Muscular Dystrophy Type 2D

Non-Communicating Isolated Syringomyelia

Arnold-Chiari Malformation Type 1

Libellé préféré : malformation d'Arnold-Chiari; Synonyme CISMeF : malformation Arnold-Chiari; Syndrome d'Arnold Chiari; Hyponyme MeSH : Malformation d'Arnold-Chiari de type I; Malformation d'Arnold-Chiari de type III; Malformation d'Arnold-Chiari de type II; Malformation d'Arnold-Chiari de type IV; Malformation[…] [cismef.org]

Ataxia-Telangiectasia-Like Disorder

In particular, it can be noticed as instability of the trunk when toddlers are sitting or as an unstable gait. [ncbi.nlm.nih.gov]

Congenital Disorder of Glycosylation Type 2K

On examination, he had severe mental retardation with no speech and an unstable gait. [jmg.bmj.com]

Congenital Disorder of Glycosylation Type 2E

On examination, he had severe mental retardation with no speech and an unstable gait. [jmg.bmj.com]