Broad-Based Gait: Causes & Reasons

Possible Causes for Broad-Based Gait

Patients with ataxic cerebral palsy will usually have a broad-based gait, i.e. they walk with their feet unusually far apart. [medhelp.org]

Showing of 9 | Percent of people who have these symptoms is not available through HPO Autosomal recessive inheritance 0000007 Broad-based gait Wide based walk 0002136 Cerebellar [rarediseases.info.nih.gov]

Tabes Dorsalis

The patient's ataxia was evident as she walked with a broad-based gait. [lksom.temple.edu]

Argyll-Robertson pupils Impaired vibratory and proprioception sense Broad base and sensory ataxic gait Positive Romberg's test Tabes dorsalis ++ ++ ++ ++ ++ ++ ++ ++ Positive [wikidoc.org]

[1][2][3][4] Diseases History and symptoms Physical examination Laboratory findings Other findings Lightning pains Impaired sensation Progressive sensory ataxia Unsteady gait [wikidoc.org]

Diabetic Pseudotabes

In addition to the broad-based, stamping gait, which becomes worse when patients try to walk in the dark, abnormal findings included diminished vision owing to optic atrophy [std-aid.com]

Ataxia of gait is evident, and results of heel-to-sin and finger-to-nose testing are abnormal. [std-aid.com]

Subacute Combined Degeneration of Spinal Cord

His gait was broad based with spinal ataxia. Decreased graphaesthesia was found on the lower limbs, the lower part of the trunk and on the upper limbs. [neuroanatomy.wisc.edu]

Friedreich Ataxia

The unsteadiness further progresses to a broad-based,… Read More mitochondrial disorders In metabolic disease: Mitochondrial disorders …iron homeostasis is present in Friedreich [britannica.com]

With progression, gait becomes broad-based, with frequent losses of balance requiring intermittent and then constant support. [doi.org]

Gait ataxia develops early and gait is characteristically unsteady, but not overtly broad-based. [academic.oup.com]

Duchenne Muscular Dystrophy

Duchenne muscular dystrophy (DMD) is a lethal, X-linked muscle-wasting disease caused by lack of dystrophin, essential for muscle fibre integrity. Despite extensive pre-clinical studies, development of an effective treatment has proved challenging. More recently, significant progress has been made with the first drug[…] [ncbi.nlm.nih.gov]

Acute Cerebellar Ataxia

A 29-year-old man developed acute cerebellar ataxia following Epstein-Barr virus infection. Serum IgG and IgM antibodies reacted with both nuclear and cytoplasmic elements of neurons. Western blot revealed IgG binding to the 34- and 29-kd bands and IgM binding to the 44-, 37-, and 29-kd bands. The IgM reactivity[…] [ncbi.nlm.nih.gov]

Aromatic L-Amino Acid Decarboxylase Deficiency

OBJECTIVE/CONTEXT: Long-fasting hypoglycemia in children may be induced by neurotransmitter disorders. A 5-year-old girl with a medical history of chronic diarrhea presented three episodes of severe hypoglycemia (20 mg/dL) between ages 3 and 5 years. She became pale and sweaty with hypothermia (33.5°C),[…] [ncbi.nlm.nih.gov]

Hereditary Areflexic Dystasia

C. Haubrich T. Krings J. Senderek S. Züchner J. Schröder J. Noth R. Töpper Diagnostic Neuroradiology Abstract. Hypertrophic radiculopathy is a rare feature of neuropathies. Single cases of enlarged nerve roots have been described in hereditary motor sensory neuropathies (HMSN) and chronic inflammatory[…] [doi.org]

Ataxia Telangiectasia

The laboratory diagnosis of ataxia-telangiectasia (A-T) currently relies upon measurement of serum alphafetoprotein (AFP) and cellular sensitivity to ionizing radiation. A previous report suggests that immunoblotting of whole cell lysates from lymphoblastoid cell lines (LCLs) might be informative for diagnosis. To[…] [ncbi.nlm.nih.gov]

Ochronosis with Alkaptonuria

Abstract A 59-year-old woman with previously documented alkaptonuria was examined for extensive ochronosis of recent onset. The cause of the extensive skin pigmentations were thought to be secondary to decreased renal clearance of homogentisic acid because of a decline in the patient's renal function. If[…] [ncbi.nlm.nih.gov]

Camurati-Engelmann Syndrome

This is observed by the broad-based gait with a duck-like waddle to the swing phase, the pelvis drops to the side of the leg being raised, notable forward curvature of the [en.wikipedia.org]

Those with the disease tend to have a very characteristic walk medically diagnosed as a 'waddling gait'. [en.wikipedia.org]

X-linked Mental Retardation Type Cabezas

[…] people have these symptoms Aggressive behavior Aggressive behaviour Aggression Aggressiveness [ more ] 0000718 Blepharophimosis Narrow opening between the eyelids 0000581 Broad-based [rarediseases.info.nih.gov]

gait Wide based walk 0002136 Cachexia Wasting syndrome 0004326 Decreased testicular size Small testes Small testis [ more ] 0008734 High palate Elevated palate Increased [rarediseases.info.nih.gov]

[…] length of neck 0000470 Short palm 0004279 Short philtrum 0000322 Small hand Disproportionately small hands 0200055 Synophrys Monobrow Unibrow [ more ] 0000664 Wide mouth Broad [rarediseases.info.nih.gov]

AP4 Deficiency Syndrome

Patient IV-7 sat unaided at 11 months of age and walked at 3 years, with a broad-based unsteady gait. [ncbi.nlm.nih.gov]

2 and IV-5 sat unaided at 7 months; patient IV-2 was able to crawl at 2 years but never managed to walk; her sister IV-5 could walk short distances with unsteady spastic gait [ncbi.nlm.nih.gov]

Cerebellar Ataxia - Mental Retardation - Dysequlibrium Syndrome

[…] is not available through HPO Abnormality of metabolism/homeostasis Laboratory abnormality Metabolism abnormality [ more ] 0001939 Autosomal recessive inheritance 0000007 Broad-based [rarediseases.info.nih.gov]

gait Wide based walk 0002136 Cerebellar atrophy Degeneration of cerebellum 0001272 Cerebellar hypoplasia Small cerebellum Underdeveloped cerebellum [ more ] 0001321 Congenital [rarediseases.info.nih.gov]

Kozlowski Warren Fisher Syndrome

Term ID: 2136 Name: Broad-based gait Synonym: Broad based gait; Wide based gait; Wide based walk; Wide-based gait Definition: An abnormal gait pattern in which persons stand [mseqdr.org]

613647 C3150901 OMIM 1 713 22197 613653 HP:0002136 HP:0002136 Broad-based gait 0 ATCAY CL E G H 85300 94122 ORPHA 1 179 779 608179 HP:0002136 HP:0002136 Broad-based gait [mseqdr.org]

HP:0002136 HP:0002136 Broad-based gait 0 CDK10 CL E G H 8558 617694 AL KAISSI SYNDROME 617694 C4540156 OMIM 1 90 1770 603464 HP:0002136 HP:0002136 Broad-based gait 0 CHD3 [mseqdr.org]

Jaberi-Elahi Syndrome

[…] weakness Hypotonia Joint hypermobility Joint stiffness Kyphosis Microcephaly Muscle weakness Pectus carinatum Scoliosis Abnormality of the nervous system Brisk reflexes Broad-based [ncbi.nlm.nih.gov]

Gait ataxia is characteirzed by a wide-based staggering gait with a tendency to fall. [ncbi.nlm.nih.gov]

gait Cerebellar vermis atrophy Choreoathetosis Dysmetria Dystonic disorder Gait ataxia Generalized tonic-clonic seizures Global developmental delay Globus pallidus hypointensity [ncbi.nlm.nih.gov]

Diffuse Corticomeningeal Angiomatosis of Divry and Van Bogaert

New England type (Broad-based gait) Angelman Syndrome (Broad-based gait) Angiomatosis, diffuse corticomeningeal, of Divry and Van Bogaert (Broad-based gait) Ataxia (Broad-based [familydiagnosis.com]

33 HP:0001123 8 migraine 33 HP:0002076 9 ventriculomegaly 33 HP:0002119 10 dementia 33 HP:0000726 11 cutis marmorata 33 HP:0000965 12 pseudobulbar signs 33 HP:0002200 13 broad-based [malacards.org]

Broad-based gait MedGen UID: 167799 • Concept ID: C0856863 • Finding An abnormal gait pattern in which persons stand and walk with their feet spaced widely apart. [ncbi.nlm.nih.gov]

Deoxyribose-5-Phosphate Aldolase Deficiency

ORPHA:79434 Angelman Syndrome Due To Maternal 15Q11Q13 Deletion Gait imbalance, Broad-based gait, Ataxia, Happy demeanor, Hyperactivity, Hypopigmentation of the ... [mousephenotype.org]

ORPHA:231222 Neurodevelopmental Disorder With Movement Abnormalities, Abnormal Gait, And Autistic Features Broad-based gait, Happy demeanor, Hyperactivity, Thick eyebrow, [mousephenotype.org]

OMIM:209950 Fanconi Renotubular Syndrome 5 Hypophosphatemic rickets, Hypophosphatemia OMIM:618913 Angelman Syndrome Due To A Point Mutation Gait imbalance, Broad-based gait [mousephenotype.org]

Intellectual Developmental Disorder with Gastrointestinal Difficulties and High Pain Threshold

Most patients have variable additional features, including feeding and gastrointestinal difficulties, high pain threshold, hypersensitivity to sound, hypotonia, broad-based [malacards.org]

gait, and dysmorphic features, including mild facial abnormalities, strabismus, and small hands and feet. [malacards.org]

Yuan-Harel-Lupski Syndrome

Gait ataxia is characteirzed by a wide-based staggering gait with a tendency to fall. [ncbi.nlm.nih.gov]

Gait, if achieved, was often unstable and broad based. [jmg.bmj.com]

Broad-based gait MedGen UID: 167799 •Concept ID: C0856863 • Finding An abnormal gait pattern in which persons stand and walk with their feet spaced widely apart. [ncbi.nlm.nih.gov]

X-Linked Spinocerebellar Ataxia Type 5

There is a broad-based gait, scanning dysarthria, explosive speech, intention tremor, dysdiadochokinesia, dysmetria and abnormalities of eye movements. [patient.info]

He was barely able to walk, with a broad-based gait. [e-jmd.org]

Autosomal Dominant Mental Retardation Type 26

Protein kinase essential for neurogenesis, neuronal differentiation, synaptic plasticity IncompleteE ID, severe speech delay/absent speech, epilepsy, ataxia/ broad-based gait [ncbi.nlm.nih.gov]

Autosomal Dominant Mental Retardation Type 1

[…] behavior aggression autistic-like symptoms* have a slow growth curve develop short stature as they age microcephaly, or small head circumference have difficulty walking a broad-based [2q23.org]

gait Children may also show various types of common facial features (listed below), and different types of skeletal or bone changes. constipation It is important to meet [2q23.org]

Snijders Blok-Campeau Syndrome

Broad-based gait MedGen UID: 167799 •Concept ID: C0856863 • Finding An abnormal gait pattern in which persons stand and walk with their feet spaced widely apart. [ncbi.nlm.nih.gov]

Hypermetropia Hypertelorism Strabismus Abnormality of the musculoskeletal system Frontal bossing Generalized hypotonia Macrocephaly Scoliosis Abnormality of the nervous system Broad-based [ncbi.nlm.nih.gov]

gait Delayed ability to walk Delayed speech and language development Dysarthria Global developmental delay Motor stereotypy Speech apraxia Stuttering Unsteady gait Ventriculomegaly [ncbi.nlm.nih.gov]

Cerebellar Ataxia Type Cayman

[from OMIM] Show allHide all Abnormality of the eye Nystagmus Abnormality of the musculoskeletal system Generalized hypotonia Hypotonia Abnormality of the nervous system Broad-based [ncbi.nlm.nih.gov]

Broad-based gait MedGen UID: 167799 • Concept ID: C0856863 • Finding An abnormal gait pattern in which persons stand and walk with their feet spaced widely apart. [ncbi.nlm.nih.gov]

gait Dysarthria Gait ataxia Global developmental delay Intention tremor IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters [ncbi.nlm.nih.gov]

GNAO1 Encephalopathy

Gait ataxia, Broad-based ga... [mousephenotype.org]

Dysdiadochokinesis, Broad-based ... [mousephenotype.org]

ORPHA:650 Myopathy, Spheroid Body Waddling gait, Broad-based gait, Tremor OMIM:182920 Dyserythropoiesis, Congenital, With Ultrastructurally Normal Erythroblast Heterochromatin [mousephenotype.org]

CHIME Syndrome

Broad-based gait MedGen UID: 167799 •Concept ID: C0856863 • Finding An abnormal gait pattern in which persons stand and walk with their feet spaced widely apart. [ncbi.nlm.nih.gov]

[…] proximal interphalangeal joint of the 5th finger Frontal bossing Generalized hypotonia Hypotonia Joint contracture of the hand Plagiocephaly Abnormality of the nervous system Broad-based [ncbi.nlm.nih.gov]

gait Cerebral atrophy Intellectual disability Seizure Violent behavior Ear malformation Conductive hearing impairment Overfolded helix Growth abnormality Growth abnormality [ncbi.nlm.nih.gov]

Wiedemann-Steiner Syndrome

[…] behavior Aggression Aggressive behaviour Aggressiveness [ more ] 0000718 Autosomal dominant inheritance 0000006 Blepharophimosis Narrow opening between the eyelids 0000581 Broad-based [rarediseases.info.nih.gov]

gait Wide based walk 0002136 Clinodactyly of the 5th finger Permanent curving of the pinkie finger 0004209 Delayed speech and language development Deficiency of speech development [rarediseases.info.nih.gov]

Dysequilibrium Syndrome