Hypertension, and Flexion contracture

Diseases related with Hypertension and Flexion contracture

In the following list you will find some of the most common rare diseases related to Hypertension and Flexion contracture that can help you solving undiagnosed cases.

Top matches:

Low match MELORHEOSTOSIS

Melorheostosis is a rare connective tissue disorder characterized by a sclerosing bone dysplasia, usually limited to one side of the body (rarely bilateral), that manifests with pain, stiffness, joint contractures and deformities.

MELORHEOSTOSIS Is also known as mel

Related symptoms:

  • Failure to thrive
  • Pain
  • Flexion contracture
  • Hypertension
  • Skeletal muscle atrophy


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about MELORHEOSTOSIS

Familial aortic dissection is the term used to describe rupture of the aortic wall at the level of the media, resulting in the formation of a false channel and deviation of part of the aortic flux. Familial predisposition to thoracic aortic aneurysms and type A dissections (concerning the ascending aorta and/or the aortic arch) has been demonstrated in around 19% of patients presenting with thoracic aortic dissections and several loci have been identified so far (16p12.2-p13.13, 3p24-25). This predisposition is transmitted in an autosomal dominant manner.

FAMILIAL AORTIC DISSECTION Is also known as aortic aneurysm, familial thoracic|annuloaortic ectasia|cystic medial necrosis of aorta|aortic dissection, familial|aneurysm, thoracic aortic|faa1

Related symptoms:

  • Cataract
  • Flexion contracture
  • Hypertension
  • Dilatation
  • Pectus excavatum


SOURCES: ORPHANET OMIM MENDELIAN

More info about FAMILIAL AORTIC DISSECTION

Related symptoms:

  • Global developmental delay
  • Generalized hypotonia
  • Hearing impairment
  • Growth delay
  • Muscle weakness


SOURCES: OMIM MENDELIAN

More info about COENZYME Q10 DEFICIENCY, PRIMARY, 8; COQ10D8

Other less relevant matches:

Related symptoms:

  • Flexion contracture
  • Hypertension
  • Ventricular septal defect
  • Atrial septal defect
  • Short nose


SOURCES: MESH OMIM MENDELIAN

More info about HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION; HCAD

X-linked myopathy with postural muscle atrophy is a rare progressive muscular dystrophy characterized by an adult-onset scapulo-axio-peroneal myopathy. Clinical presentation includes shoulder girdle atrophy, scapular winging, axial muscular atrophy of postural muscles combined with a generalized hypertrophy. Typically, neck rigidity, rigid spine, Achilles tendon shortening, and respiratory insufficiency later in disease course are present.

X-LINKED MYOPATHY WITH POSTURAL MUSCLE ATROPHY Is also known as xmpma

Related symptoms:

  • Scoliosis
  • Muscle weakness
  • Pain
  • Ptosis
  • Flexion contracture


SOURCES: OMIM ORPHANET MENDELIAN

More info about X-LINKED MYOPATHY WITH POSTURAL MUSCLE ATROPHY

Related symptoms:

  • Scoliosis
  • Growth delay
  • Hypertelorism
  • Micrognathia
  • Abnormal facial shape


SOURCES: OMIM MENDELIAN

More info about LETHAL CONGENITAL CONTRACTURE SYNDROME 9; LCCS9

Autosomal dominant dopa-responsive dystonia (DYT5a) is a rare neurometabolic disorder characterized by childhood-onset dystonia that shows a dramatic and sustained response to low doses of levodopa (L-dopa) and that may be associated with parkinsonism at an older age.

AUTOSOMAL DOMINANT DOPA-RESPONSIVE DYSTONIA Is also known as hpd with marked diurnal fluctuation|gtpch1-deficient dopa-responsive dystonia|gtpch1-deficient drd|dyt5a|hereditary progressive dystonia with marked diurnal fluctuation|autosomal dominant segawa syndrome

Related symptoms:

  • Intellectual disability
  • Hearing impairment
  • Scoliosis
  • Ataxia
  • Hypertension


SOURCES: ORPHANET MENDELIAN

More info about AUTOSOMAL DOMINANT DOPA-RESPONSIVE DYSTONIA

GLYCOGEN STORAGE DISEASE IV; GSD4 Is also known as andersen disease|brancher deficiency|gbe1 deficiency|amylopectinosis|gsd iv|glycogen branching enzyme deficiency|cirrhosis, familial, with deposition of abnormal glycogen|glycogenosis iv

Related symptoms:

  • Generalized hypotonia
  • Failure to thrive
  • Muscle weakness
  • Muscular hypotonia
  • Flexion contracture


SOURCES: OMIM MENDELIAN

More info about GLYCOGEN STORAGE DISEASE IV; GSD4

HOMOZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA Is also known as hofh

Related symptoms:

  • Hypertension
  • Dyspnea
  • Arthralgia
  • Hepatic steatosis
  • Sudden cardiac death


SOURCES: ORPHANET MENDELIAN

More info about HOMOZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA

Diffuse cutaneous systemic sclerosis (dcSSc) is a subtype of Systemic Sclerosis (SSc; see this term) characterized by truncal and acral skin fibrosis with an early and significant incidence of diffuse involvement (interstitial lung disease, oliguric renal failure, diffuse gastrointestinal disease, and myocardial involvement).

DIFFUSE CUTANEOUS SYSTEMIC SCLEROSIS Is also known as progressive cutaneous systemic scleroderma|diffuse cutaneous systemic scleroderma|progressive cutaneous systemic sclerosis

Related symptoms:

  • Muscle weakness
  • Pain
  • Flexion contracture
  • Hypertension
  • Dysphagia


SOURCES: ORPHANET MENDELIAN

More info about DIFFUSE CUTANEOUS SYSTEMIC SCLEROSIS

Top 5 symptoms//phenotypes associated to Hypertension and Flexion contracture

Symptoms // Phenotype % cases
Pain Uncommon - Between 30% and 50% cases
Muscle weakness Uncommon - Between 30% and 50% cases
Dyspnea Uncommon - Between 30% and 50% cases
Talipes equinovarus Uncommon - Between 30% and 50% cases
Scoliosis Uncommon - Between 30% and 50% cases

Other less frequent symptoms

Patients with Hypertension and Flexion contracture. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases

Myopathy Arthralgia Congestive heart failure Dilatation Skeletal muscle atrophy

Rare Symptoms - Less than 30% cases

Respiratory failure Rigidity Coronary artery atherosclerosis Cardiomyopathy Exertional dyspnea Dysphagia Failure to thrive Peripheral arterial stenosis Left ventricular failure Patent ductus arteriosus Generalized hypotonia Hearing impairment Growth delay Muscular hypotonia Intrauterine growth retardation Pulmonary hypoplasia Sudden cardiac death Muscular dystrophy Proximal muscle weakness Arthrogryposis multiplex congenita Polyhydramnios Edema Decreased fetal movement Scleroderma Arthritis Parkinsonism Abnormality of the substantia nigra Paresis of extensor muscles of the big toe Peripheral neuropathy Hepatomegaly Hyporeflexia Abnormality of the diaphragm Hepatosplenomegaly Thoracic kyphoscoliosis Preeclampsia Ulnar deviation of the hand Short umbilical cord Difficulty walking Hyperlordosis Abnormality of the liver Dilated cardiomyopathy Limb muscle weakness Cirrhosis Hepatic failure Ascites Cardiorespiratory arrest Transient hyperphenylalaninemia Progressive flexion contractures Decreased CSF homovanillic acid Hydrops fetalis Abnormality of extrapyramidal motor function Horizontal nystagmus Torticollis Rheumatoid arthritis Sleep disturbance Obsessive-compulsive behavior Postural tremor Brisk reflexes Anxiety Lower limb hyperreflexia Hypothyroidism Bradykinesia Gait ataxia Impaired vibration sensation in the lower limbs Limb dystonia Pes cavus Babinski sign Depressivity Fatigue Generalized dystonia Focal dystonia Ataxia Intellectual disability Waddling gait Difficulty climbing stairs Hepatic fibrosis Nausea and vomiting Cerebral artery atherosclerosis Myocardial steatosis Abnormal internal carotid artery morphology Abnormal eye physiology Vomiting Diarrhea Renal insufficiency Constipation Weight loss Gastroesophageal reflux Autoimmunity Carious teeth Malabsorption Abnormality of the skin Aortic atherosclerosis Pulmonary arterial hypertension Telangiectasia Skin ulcer Osteolysis Pulmonary fibrosis Telangiectasia of the skin Xerostomia Pulmonary infiltrates Osteolytic defects of the phalanges of the hand Oliguria Dyspareunia Decreased urine output Hypertensive crisis Narrow foramen obturatorium Abnormal tendon morphology Premature arteriosclerosis Decreased liver function Mitral regurgitation Exercise intolerance Reduced tendon reflexes Portal hypertension Limb-girdle muscular dystrophy Akinesia Myopathic facies Bilateral talipes equinovarus Fetal akinesia sequence Esophageal varix Generalized edema Tubulointerstitial fibrosis Limb joint contracture Hepatic steatosis Myocardial infarction Hyperlipidemia Abnormality of nervous system physiology Hypercholesterolemia Heart murmur Optic neuropathy Angina pectoris Xanthomatosis Precocious atherosclerosis Increased LDL cholesterol concentration Premature coronary artery atherosclerosis Renal artery stenosis Supravalvular aortic stenosis Tendon xanthomatosis Renal steatosis Calcification of the aorta Coronary artery aneurysm Ankylosis Micrognathia Congenital contracture Aortic dissection Chest pain Cardiomegaly Coarctation of aorta Aortic valve stenosis Atherosclerosis Aortic regurgitation Bicuspid aortic valve Aortic aneurysm Cutis marmorata Hypoplastic left heart Aortic root aneurysm Dilatation of the cerebral artery Thoracic aortic aneurysm Stroke Abdominal aortic aneurysm Ascending aortic dissection Cystic medial necrosis Carotid artery dilatation Descending thoracic aorta aneurysm Descending aortic dissection Paroxysmal dyspnea Cystic medial necrosis of the aorta Iris flocculi Global developmental delay Feeding difficulties Visual impairment Retinal detachment Coloboma Respiratory distress Hyperostosis Abnormality of the skeletal system Skeletal dysplasia Joint stiffness Abnormality of the foot Nevus Lymphedema Bone pain Increased bone mineral density Cranial nerve paralysis Hemangioma Growth abnormality Dermal atrophy Joint swelling Pectus excavatum Abnormality of the vasculature Atypical scarring of skin Lower limb asymmetry Lack of skin elasticity Prominent superficial veins Chronic pain Upper limb asymmetry Peripheral arteriovenous fistula Subcutaneous calcification Osteopoikilosis Ectopic ossification in muscle tissue Cataract Motor delay Postnatal growth retardation Pterygium Limited neck flexion Ventricular hypertrophy Left ventricular hypertrophy Scapular winging Dysphonia Back pain Skeletal muscle hypertrophy Spinal rigidity Rimmed vacuoles Limb-girdle muscle weakness Axial muscle weakness Stiff neck Scapuloperoneal weakness Hip flexor weakness Elevated serum creatine phosphokinase Hypertelorism Abnormal facial shape Low-set ears Depressed nasal bridge Anteverted nares Kyphoscoliosis Thin upper lip vermilion Camptodactyly Talipes Triangular face Joint contracture of the hand Adducted thumb Hypertrophic cardiomyopathy Arrhythmia Small for gestational age Micropenis Polyneuropathy Peripheral demyelination Oligohydramnios Renal hypoplasia Renal dysplasia Progressive muscle weakness Elevated serum creatinine Abnormal renal corticomedullary differentiation Ventricular septal defect Atrial septal defect Short nose Posteriorly rotated ears Prominent nasal bridge Respiratory insufficiency Tachycardia Bulbous nose Tapered finger Status epilepticus Aganglionic megacolon Abnormal autonomic nervous system physiology Cupped ear Agitation Hyperconvex nail Contractures of the interphalangeal joint of the thumb Ptosis Gait disturbance Short neck Abnormal bowel sounds


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