Broad-Based Gait: Causes & Reasons

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Possible Causes for Broad-Based Gait

Ataxic Cerebral Palsy

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]

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

During adolescence, the gait becomes progressively unsteady—frequently interpreted as clumsiness. [britannica.com]

Duchenne Muscular Dystrophy

Duchenne muscular dystrophy (DMD) is a recessive X-linked form of muscular dystrophy, caused by a mutation in the dystrophin gene. The presentation varies according to the age. The milestones related to mobility like walking, crawling and climbing steps are all delayed compared to a typical toddler. Large and bulky[…] [symptoma.com]

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

Ataxia telangiectasia (AT) is a rare neurodegenerative disorder inherited through an autosomal recessive pattern, mainly characterized by a progressive neurologic impairment together with cerebellar ataxia. The severity of AT varies between the subjects. Ataxia is undoubtedly one of the most important sings, and[…] [symptoma.com]

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]

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]

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]

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]

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]

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]

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]

Biemond Syndrome

In 1934, Biemond described a 58-year-old woman suffering from severe cerebellar ataxia with unsteady, broad-based gait, mild dysdiadochokinesia, and dysmetria that started [accesspediatrics.mhmedical.com]

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]

Joubert Syndrome Type 16

Increasing evidence suggests that congenital ataxia with broad-based gait, abnormal eye movement, decreased muscle tone, neonatal intermittent dyspnea or pause, mental retardation [journals.lww.com]

Dysequilibrium Syndrome

Pitt-Hopkins-Like Syndrome Type 1

[…] skull 0000248 Broad-based gait Wide based walk 0002136 Bruxism Teeth grinding 0003763 Cerebral cortical atrophy Decrease in size of the outer layer of the brain due to loss [rarediseases.info.nih.gov]

] 0000486 5%-29% of people have these symptoms Aggressive behavior Aggression Aggressive behaviour Aggressiveness [ more ] 0000718 Autism 0000717 Brachycephaly Short and broad [rarediseases.info.nih.gov]

X-Linked Syndromic Mental Retardation Type Snyder-Robinson

[…] available through HPO Abnormality of the pinna Abnormally shaped ears Auricular malformation Deformed ears Malformed ears Simple ears [ more ] 0000377 Bifid uvula 0000193 Broad-based [rarediseases.info.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]

Pointed chin Tall stature Aganglionic megacolon Intellectual disability, profound Camptodactyly of finger Protruding ear Joint laxity Thin upper lip vermilion Fine hair Broad-based [mendelian.co]

Joubert Syndrome Type 14

Dystonia with Cerebellar Atrophy (DYTCA)

Facial grimacing Vertigo Hypoplasia of the brainstem Abnormality of the eye Abnormality of movement Arachnodactyly Poor speech Pachygyria Abnormality of vision Cerebral palsy Broad-based [mendelian.co]

gait Toe walking Pes planus Cortical gyral simplification Scissor gait Hepatomegaly Splenomegaly Talipes equinovarus Intellectual disability, mild Hepatosplenomegaly Hepatic [mendelian.co]

Cerebellar Disease

No- differentiates a cerebellar broad based gait from a sensory broad based gait. How is the speech in cerebellar syndrome described? [brainscape.com]

OPCA Toxic/metabolic diseases Hypothyroidism & normal pressure hydrocephalus Ataxic Dysarthria: Neuromotor Deficits Hypotonia and reduced resistance to passive movement Broad-based [ucs.louisiana.edu]

Stance – a broad-based gait is noted in cerebellar disease 2. [geekymedics.com]

Odonto-Onycho-Hypohidrotic Dysplasia-Midline Scalp Defects Syndrome

[…] valve morphology Advanced eruption of teeth Rectal prolapse Premature loss of primary teeth Abnormal diaphysis morphology Thick nasal alae Coxa valga Decreased body weight Broad-based [mendelian.co]

gait Periorbital fullness Depressed nasal bridge Recurrent pyelonephritis Fulminant hepatic failure Hair-pulling Tongue thrusting Hyperorality Cerebellar cortical atrophy [mendelian.co]

Joubert Syndrome Type 20

Muscular Dystrophy-Dystroglycanopathy Type C4

Showing of 23 | 30%-79% of people have these symptoms Broad-based gait Wide based walk 0002136 Calf muscle hypertrophy Increased size of calf muscles 0008981 Delayed speech [rarediseases.info.nih.gov]