Congestive heart failure, and Abnormality of movement

Diseases related with Congestive heart failure and Abnormality of movement

In the following list you will find some of the most common rare diseases related to Congestive heart failure and Abnormality of movement that can help you solving undiagnosed cases.


Top matches:

Low match GLUCOCORTICOID DEFICIENCY 5; GCCD5


Familial glucocorticoid deficiency-5 is characterized by resistance to adrenocorticotropic hormone (ACTH) and isolated glucocorticoid deficiency, with typical biochemical findings of low serum cortisol levels and high plasma ACTH. Patients commonly present with hyperpigmentation (Prasad et al., 2014).For a discussion of genetic heterogeneity of familial glucocorticoid deficiency, see GCCD1 (OMIM ).

Related symptoms:

  • Ventricular septal defect
  • Congestive heart failure
  • Truncus arteriosus


SOURCES: OMIM MENDELIAN

More info about GLUCOCORTICOID DEFICIENCY 5; GCCD5

Low match ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 13; ARVD13


Arrhythmogenic right ventricular cardiomyopathy/dysplasia is characterized by progressive fibrofatty myocardial replacement, primarily of the right ventricle. The main clinical features are structural and functional abnormalities of the ventricles, electrocardiographic depolarization/repolarization changes, reentrant arrhythmias, and sudden death (summary by van Hengel et al., 2013).

ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 13; ARVD13 Is also known as arvc13|arrhythmogenic right ventricular cardiomyopathy 13

Related symptoms:

  • Cardiomyopathy
  • Congestive heart failure
  • Arrhythmia
  • Tachycardia
  • Syncope


SOURCES: OMIM MENDELIAN

More info about ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 13; ARVD13

Low match ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5; ARVD5


ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5; ARVD5 Is also known as arrhythmogenic right ventricular cardiomyopathy 5|arvc5

Related symptoms:

  • Cardiomyopathy
  • Congestive heart failure
  • Dilated cardiomyopathy
  • Dyskinesia
  • Chest pain


SOURCES: MESH OMIM MENDELIAN

More info about ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5; ARVD5

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Other less relevant matches:

Low match CARDIOMYOPATHY, DILATED, 1D; CMD1D


CARDIOMYOPATHY, DILATED, 1D; CMD1D Is also known as left ventricular noncompaction 6, included|lvnc6, included

Related symptoms:

  • Ventriculomegaly
  • Cardiomyopathy
  • Congestive heart failure
  • Dilatation
  • Dyspnea


SOURCES: OMIM MESH MENDELIAN

More info about CARDIOMYOPATHY, DILATED, 1D; CMD1D

Low match LONG QT SYNDROME 13; LQT13


Congenital long QT syndrome is electrocardiographically characterized by a prolonged QT interval and polymorphic ventricular arrhythmias (torsade de pointes). These cardiac arrhythmias may result in recurrent syncope, seizure, or sudden death (Jongbloed et al., 1999).For a discussion of genetic heterogeneity of long QT syndrome, see LQT1 (OMIM ).

Related symptoms:

  • Seizures
  • Hypertension
  • Congestive heart failure
  • Arrhythmia
  • Paralysis


SOURCES: OMIM MENDELIAN

More info about LONG QT SYNDROME 13; LQT13

Low match ATAXIA, SENSORY, 1, AUTOSOMAL DOMINANT; SNAX1


ATAXIA, SENSORY, 1, AUTOSOMAL DOMINANT; SNAX1 Is also known as adsa

Related symptoms:

  • Ataxia
  • Dysarthria
  • Gait disturbance
  • Dysphagia
  • Congestive heart failure


SOURCES: OMIM MENDELIAN

More info about ATAXIA, SENSORY, 1, AUTOSOMAL DOMINANT; SNAX1

Low match FAMILIAL DYSKINESIA AND FACIAL MYOKYMIA


Familial dyskinesia and facial myokymia is a rare paroxysmal movement disorder, with childhood or adolescent onset, characterized by paroxysmal choreiform, dystonic, and myoclonic movements involving the limbs (mostly distal upper limbs), neck and/or face, which can progressively increase in both frequency and severity until they become nearly constant. Patients may also present with delayed motor milestones, perioral and periorbital dyskinesias, dysarthria, hypotonia, and weakness.

FAMILIAL DYSKINESIA AND FACIAL MYOKYMIA Is also known as fdfm

Related symptoms:

  • Intellectual disability
  • Generalized hypotonia
  • Motor delay
  • Hyperreflexia
  • Dysarthria


SOURCES: ORPHANET MESH OMIM MENDELIAN

More info about FAMILIAL DYSKINESIA AND FACIAL MYOKYMIA

Low match WOLFF-PARKINSON-WHITE SYNDROME


A group of conditions in which HEART VENTRICLE activation by the atrial impulse is faster than the normal impulse conduction from the SINOATRIAL NODE. In these pre-excitation syndromes, atrial impulses often bypass the ATRIOVENTRICULAR NODE delay and travel via ACCESSORY CONDUCTING PATHWAYS connecting the atrium directly to the BUNDLE OF HIS.

WOLFF-PARKINSON-WHITE SYNDROME Is also known as wpw syndrome

Related symptoms:

  • Pain
  • Respiratory distress
  • Cardiomyopathy
  • Congestive heart failure
  • Arrhythmia


SOURCES: OMIM ORPHANET MENDELIAN

More info about WOLFF-PARKINSON-WHITE SYNDROME

Low match DESMINOPATHY


Desminopathy is a rare genetic skeletal muscle disease characterized by abnormal chimeric aggregates of desmin and other cytoskeletal proteins and granulofilamentous material at the ultrastructural level in muscle biopsies and variable clinical/ myopathological features, age of disease onset and rate of disease progression. Patients present with bilateral skeletal muscle weakness that starts in distal leg muscles and spreads proximally, sometimes involving trunk, neck flexors and facial muscles and often cardiomyopathy manifested by conduction blocks, arrhythmias, chronic heart failure, and sometimes tachyarrhythmia. Weakness eventually leads to wheelchair dependence. Respiratory insufficiency can be a major cause of disability and death, beginning with nocturnal hyperventilation with oxygen desaturation and progressing to daytime respiratory failure.

DESMINOPATHY Is also known as desmin-related myofibrillar myopathy

Related symptoms:

  • Cardiomyopathy
  • Diarrhea
  • Arrhythmia
  • Constipation
  • Proximal muscle weakness


SOURCES: ORPHANET MENDELIAN

More info about DESMINOPATHY

Top 5 symptoms//phenotypes associated to Congestive heart failure and Abnormality of movement

Symptoms // Phenotype % cases
Cardiomyopathy Common - Between 50% and 80% cases
Arrhythmia Uncommon - Between 30% and 50% cases
Syncope Uncommon - Between 30% and 50% cases
Dilated cardiomyopathy Uncommon - Between 30% and 50% cases
Sudden cardiac death Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

Patients with Congestive heart failure and Abnormality of movement. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases


Tachycardia Ventricular tachycardia Atrioventricular block Atrial fibrillation Right ventricular cardiomyopathy Chest pain Hypokinesia Abnormal EKG Palpitations Right bundle branch block

Rare Symptoms - Less than 30% cases


Anxiety Cardiac arrest Dyspnea Dilatation Paroxysmal atrial fibrillation Cardiomegaly Dysarthria Pain Prolonged QRS complex Dyskinesia Right ventricular dilatation Hypertrophic cardiomyopathy Left bundle branch block Bundle branch block Hypotension Ventricular preexcitation with multiple accessory pathways EMG: myopathic abnormalities Respiratory insufficiency due to muscle weakness Distal muscle weakness Facial palsy Proximal muscle weakness Respiratory distress Constipation Diarrhea Abnormal heart morphology Shortened PR interval Paroxysmal supraventricular tachycardia Ventricular preexcitation Neck muscle weakness Atrial flutter Wolff-Parkinson-White syndrome Supraventricular tachycardia Muscle fibrillation Stroke Vertigo Ventricular fibrillation Bulbar palsy Ventricular septal defect Skeletal myopathy Reduced number of teeth Gingival recession Reduced systolic function Selective tooth agenesis Leukonychia Myocardial fibrosis Woolly hair Fragile nails Parakeratosis Agenesis of permanent teeth Aplasia/Hypoplasia of the eyebrow Loss of consciousness Absent eyebrow Oligodontia Hyporeflexia of lower limbs Palmoplantar keratoderma Ichthyosis Facial myokymia Nail dystrophy Pruritus Erythema Hyperkeratosis Trifascicular block Restrictive heart failure Late-onset proximal muscle weakness Left anterior fascicular block Abnormal levels of creatine kinase in blood Carious teeth Dystonia Paroxysmal dyskinesia Postural instability Babinski sign Hyporeflexia Areflexia Dysphagia Gait disturbance Ataxia Torsade de pointes Pulmonary embolism Prolonged QT interval Coronary artery atherosclerosis Ventricular arrhythmia Paralysis Falls Hypertension Seizures Left ventricular noncompaction Left ventricular hypertrophy Ventriculomegaly Presyncope Ventricular extrasystoles Abnormal T-wave Abnormal echocardiogram Reduced ejection fraction Akinesia Truncus arteriosus Dysmetria Distal sensory impairment Orofacial dyskinesia Hypertonia Myokymia Limb hypertonia Resting tremor Delayed gross motor development Involuntary movements Choreoathetosis Chorea Muscular hypotonia of the trunk Difficulty walking Myoclonus Tremor Abnormal cerebellum morphology Hyperreflexia Motor delay Generalized hypotonia Intellectual disability Gait instability, worse in the dark Distal sensory impairment of all modalities Distal sensory loss of all modalities Positive Romberg sign Sensory ataxia Peripheral demyelination Neuronal loss in central nervous system Gliosis Agenesis of molar



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