Hydrocephalus, and Pulmonary arterial hypertension

Diseases related with Hydrocephalus and Pulmonary arterial hypertension

In the following list you will find some of the most common rare diseases related to Hydrocephalus and Pulmonary arterial hypertension that can help you solving undiagnosed cases.

Top matches:

Severe achondroplasia-developmental delay-acanthosis nigricans syndrome is characterised by the association of severe achondroplasia with developmental delay and acanthosis nigricans. It has been described in four unrelated individuals. Structural central nervous system anomalies, seizures and hearing loss were also reported, together with bowing of the clavicle, femur, tibia and fibula in some cases. The syndrome is caused by a Lys650Met substitution in the kinase domain of fibroblast growth factor receptor 3 (encoded by the FGFR3 gene; 4p16.3).

SEVERE ACHONDROPLASIA-DEVELOPMENTAL DELAY-ACANTHOSIS NIGRICANS SYNDROME Is also known as saddan|saddan dysplasia

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Hearing impairment


SOURCES: ORPHANET OMIM MENDELIAN

More info about SEVERE ACHONDROPLASIA-DEVELOPMENTAL DELAY-ACANTHOSIS NIGRICANS SYNDROME

Infantile malignant osteopetrosis is a rare congenital disorder of bone resorption characterised by generalised skeletal densification.

AUTOSOMAL RECESSIVE MALIGNANT OSTEOPETROSIS Is also known as infantile malignant osteopetrosis|osteopetrosis, infantile malignant 2

Related symptoms:

  • Seizures
  • Short stature
  • Hearing impairment
  • Growth delay
  • Nystagmus


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about AUTOSOMAL RECESSIVE MALIGNANT OSTEOPETROSIS

Mucopolysaccharidosis type 2 (MPS2, see this term), severe form (MPS2S), is associated with a massive accumulation of glycosaminoglycans and a wide variety of symptoms including a rapidly progressive cognitive decline; it is most often fatal in the second or third decade.

MUCOPOLYSACCHARIDOSIS TYPE 2, SEVERE FORM Is also known as mucopolysaccharidosis type ii, severe form|mps2a|iduronate 2-sulfatase deficiency type a|mucopolysaccharidosis type 2a|hunter syndrome type a|mpsiia|mucopolysaccharidosis type iia

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Hearing impairment


SOURCES: ORPHANET MENDELIAN

More info about MUCOPOLYSACCHARIDOSIS TYPE 2, SEVERE FORM

Other less relevant matches:

Encephalocraniocutaneous lipomatosis (ECCL) is a neurocutaneous disorder characterized by ocular anomalies, skin lesions, and central nervous system (CNS) anomalies (Moog et al., 2007).The malformations in ECCL are patchy and asymmetric. The most characteristic skin anomaly is nevus psiloliparus, a well-demarcated, alopecic fatty tissue nevus on the scalp, seen in 80% of affected individuals. Other dermatologic features include frontotemporal or zygomatic subcutaneous fatty lipomas, non-scarring alopecia, focal dermal hypoplasia or aplasia of the scalp, periocular skin tags, and pigmentary abnormalities following the lines of Blaschko. Choristomas of the eye (epibulbar dermoids or lipodermoids) are also present in 80% of patients, and can be unilateral or bilateral. Characteristic CNS features in ECCL include intracranial and intraspinal lipomas, seen in 61% of patients, and less often cerebral asymmetry, arachnoid cysts, enlarged ventricles, and leptomeningeal angiomatosis. A predisposition to low-grade gliomas has also been observed. Seizures and intellectual disability are common, but one-third of affected individuals have normal intellect. Skeletal manifestations include bone cysts and jaw tumors, such as odontomas, osteomas, and ossifying fibromas (summary by Bennett et al., 2016).

ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS Is also known as haberland syndrome

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Neoplasm
  • Failure to thrive


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS

Combined methylmalonic aciduria (MMA) and homocystinuria is a genetically heterogeneous disorder of cobalamin (cbl; vitamin B12) metabolism. The defect causes decreased levels of the coenzymes adenosylcobalamin (AdoCbl) and methylcobalamin (MeCbl), which results in decreased activity of the respective enzymes methylmalonyl-CoA mutase (MUT ) and methyltetrahydrofolate:homocysteine methyltransferase, also known as methionine synthase (MTR ). Different forms of the disorder have been classified according to complementation groups of cells in vitro: cblC, cblD (OMIM ), cblF (OMIM ), and cblJ (OMIM ).Isolated methylmalonic acidurias have also been classified by complementation groups: MMA 'mut' (OMIM ) is caused by mutation in the MUT gene on chromosome 6p21; MMA cblA (OMIM ) is caused by mutation in the MMAA gene (OMIM ) on 4q31; and MMA cblB (OMIM ) is caused by mutation in the MMAB gene (OMIM ) on 12q24.Methylmalonic aciduria and homocystinuria, cblC type, is the most common inborn error of vitamin B12 (cobalamin) metabolism, with about 250 known cases (Lerner-Ellis et al., 2006). Affected individuals may have developmental, hematologic, neurologic, metabolic, ophthalmologic, and dermatologic clinical findings. Although considered a disease of infancy or childhood, some individuals develop symptoms in adulthood (Rosenblatt et al., 1997).

METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC Is also known as vitamin b12 metabolic defect with combined deficiency of methylmalonyl-coa mutase and homocysteine:methyltetrahydrofolate methyltransferase|methylmalonic aciduria and homocystinuria, vitamin b12-responsive|methylmalonic acidemia and homocystinuria, cblc t

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Hearing impairment


SOURCES: ORPHANET OMIM MENDELIAN

More info about METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC

Adams-Oliver Syndrome (AOS) is a rare disorder characterized by the combination of congenital limb abnormalities and scalp defects, often accompanied by skull ossification defects.

ADAMS-OLIVER SYNDROME Is also known as aplasia cutis congenita with terminal transverse limb defects|congenital scalp defects with distal limb reduction anomalies|congenital scalp defects with distal limb anomalies|aos|absence defect of limbs, scalp, and skull|limb, scalp and skull defects

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Microcephaly


SOURCES: ORPHANET OMIM MENDELIAN

More info about ADAMS-OLIVER SYNDROME

Gaucher disease type 3 is the subacute neurological form of Gaucher disease (GD; see this term) characterized by progressive encephalopathy and associated with the systemic manifestations (organomegaly, bone involvement, cytopenia) of GD type 1 (see this term).

GAUCHER DISEASE TYPE 3 Is also known as chronic neuronopathic gaucher disease|cerebral juvenile and adult form of gaucher disease|gaucher disease, subacute neuronopathic type

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Scoliosis


SOURCES: ORPHANET MENDELIAN

More info about GAUCHER DISEASE TYPE 3

Gorlin-Chaudhry-Moss (GCM) syndrome is a multiple congenital anomaly syndrome characterized by craniofacial dysostosis, facial dysmorphism, conductive hearing loss, generalized hypertrichosis, and extremity, ocular and dental anomalies.

GORLIN-CHAUDHRY-MOSS SYNDROME Is also known as gcm syndrome|gorlin-chaudhry-moss syndrome|craniofacial dysostosis, hypertrichosis, hypoplasia of labia majora, dental and eye anomalies, patent ductus arteriosus, and normal intelligence|craniofacial dysostosis-genital, dental, cardiac anomalies syndrome

Related symptoms:

  • Global developmental delay
  • Short stature
  • Generalized hypotonia
  • Hearing impairment
  • Microcephaly


SOURCES: OMIM ORPHANET MENDELIAN

More info about GORLIN-CHAUDHRY-MOSS SYNDROME

Yunis-Varon syndrome is a severe autosomal recessive disorder characterized by skeletal defects, including cleidocranial dysplasia and digital anomalies, and severe neurologic involvement with neuronal loss. Enlarged cytoplasmic vacuoles are found in neurons, muscle, and cartilage. The disorder is usually lethal in infancy (summary by Campeau et al., 2013).

YUNIS-VARON SYNDROME Is also known as cleidocranial dysplasia with micrognathia, absent thumbs, and distal aphalangia|cleidocranial dysplasia-micrognathia-absent thumbs syndrome

Related symptoms:

  • Intellectual disability
  • Global developmental delay
  • Short stature
  • Generalized hypotonia
  • Hearing impairment


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about YUNIS-VARON SYNDROME

Related symptoms:

  • Hypertension
  • Ventriculomegaly
  • Congestive heart failure
  • Arrhythmia
  • Dilated cardiomyopathy


SOURCES: OMIM MENDELIAN

More info about LEFT VENTRICULAR NONCOMPACTION 8; LVNC8

Top 5 symptoms//phenotypes associated to Hydrocephalus and Pulmonary arterial hypertension

Symptoms // Phenotype % cases
Global developmental delay Common - Between 50% and 80% cases
Seizures Common - Between 50% and 80% cases
Intellectual disability Common - Between 50% and 80% cases
Failure to thrive Common - Between 50% and 80% cases
Hearing impairment Common - Between 50% and 80% cases

Other less frequent symptoms

Patients with Hydrocephalus and Pulmonary arterial hypertension. may also develop some of the following symptoms:

Common Symptoms - More than 50% cases

Growth delay

Uncommon Symptoms - Between 30% and 50% cases

Microcephaly Hypoplasia of the corpus callosum Short stature Hypertension Generalized hypotonia Nystagmus Ventriculomegaly Atrial septal defect Microphthalmia Low-set ears Hepatomegaly Macrocephaly Cerebellar hypoplasia Congestive heart failure Depressed nasal bridge Anemia Proptosis Tremor Pancytopenia Hypertonia Hepatosplenomegaly Small nail Ventricular septal defect Cryptorchidism Abnormality of the skull Pachygyria Sclerocornea Thrombocytopenia Syndactyly Abnormal heart morphology Kyphosis Edema Muscular hypotonia Cataract Craniosynostosis Feeding difficulties Abnormality of the skeletal system Anteverted nares Postnatal growth retardation Sparse hair Ascites Intrauterine growth retardation

Rare Symptoms - Less than 30% cases

Retinopathy Pericardial effusion Rigidity Cerebral cortical atrophy Protruding tongue Agenesis of corpus callosum Recurrent urinary tract infections Umbilical hernia Aggressive behavior Alopecia Cyanosis Abnormality of the face Brachydactyly Strabismus Respiratory distress Corneal opacity Depressivity Abnormal eyelid morphology Macrotia High forehead Narrow mouth Thin upper lip vermilion Dementia Respiratory insufficiency Difficulty walking Porencephalic cyst Sparse scalp hair Cerebellar vermis hypoplasia Abnormal facial shape Muscle weakness Ataxia Abnormality of the pinna Anonychia Micropenis Hypotrichosis Osteolysis Hematuria Dandy-Walker malformation Hypertelorism Coarctation of aorta Micrognathia Hemiparesis Aortic valve stenosis Hemiplegia Proteinuria Absent nipple Smooth philtrum Cortical dysplasia Malabsorption Aplasia cutis congenita Hip dislocation Mental deterioration Dyspnea Mitral regurgitation Mandibular prognathia Portal hypertension Bone pain Short distal phalanx of finger Premature birth Sepsis Lymphadenopathy Pallor Recurrent respiratory infections Leukopenia Splenomegaly Optic atrophy Visual impairment Bicuspid aortic valve Abnormality of the metacarpal bones Delayed skeletal maturation Cirrhosis Arrhythmia Redundant skin Wide anterior fontanel Scoliosis Otitis media Platyspondyly Severe global developmental delay Skeletal dysplasia Gastroesophageal reflux Respiratory failure Midface retrusion Intellectual disability, severe Frontal bossing Increased bone mineral density Tetralogy of Fallot High, narrow palate Osteopenia Premature loss of primary teeth Abnormal cardiac septum morphology Abnormal pulmonary valve morphology Hydrops fetalis Toe syndactyly Behavioral abnormality Patent ductus arteriosus Pulmonary artery stenosis Hernia Diarrhea Dystonia Encephalopathy Brachycephaly Menorrhagia Abnormality of the thorax Posteriorly rotated ears Osteoporosis Myoclonus Intellectual disability, mild Long philtrum Clubbing Abdominal pain Vomiting Abnormality of the foot Abnormality of the dentition Short nose Intention tremor Cholelithiasis Progressive neurologic deterioration Abnormality of the eye Synophrys Hypermetropia Broad forehead Oculomotor apraxia Cutis marmorata telangiectatica congenita Increased susceptibility to fractures Decreased body weight Periventricular cysts Imperforate hymen Acrania Dysphagia Aplasia cutis congenita over posterior parietal area Aplasia cutis congenita on trunk or limbs Conductive hearing impairment Hypoalbuminemia Retrognathia Myopia Gait disturbance Pulmonary fibrosis Fatigue Downslanted palpebral fissures Abnormality of the sternum Bulbar palsy Abnormality of the spleen Progressive cerebellar ataxia Aortic valve calcification Abnormal bleeding Spontaneous hematomas Abnormal thrombosis Generalized osteosclerosis Astrocytosis Protein-losing enteropathy Restrictive deficit on pulmonary function testing Avascular necrosis of the capital femoral epiphysis Abnormal myocardium morphology Abnormal saccadic eye movements Multiple myeloma Supranuclear gaze palsy Hypercoagulability Vertebral compression fractures Slow saccadic eye movements Thoracic kyphosis Hepatocellular carcinoma Aseptic necrosis Abnormal heart valve morphology Exertional dyspnea Lower limb hyperreflexia Mitral valve calcification Opisthotonus Horizontal supranuclear gaze palsy Abnormal pyramidal sign Generalized tonic-clonic seizures Sleep myoclonus Abnormality of the acoustic reflex Petechiae Ophthalmoplegia Abnormality of ion homeostasis Cardiac valve calcification Epistaxis Delayed puberty Hematological neoplasm Generalized myoclonic seizures Decreased beta-glucocerebrosidase protein and activity Erlenmeyer flask deformity of the femurs Lymphopenia Syncope Abnormality of eye movement Neurodegeneration Abdominal distention Orthopnea Restrictive ventilatory defect Interstitial pulmonary abnormality Abnormal retinal morphology Increased antibody level in blood Pneumothorax Astigmatism Aplasia/Hypoplasia of the nipples Abnormality of finger Hypoplastic labia majora Hypoplastic scapulae Decreased skull ossification Abnormality of the neck Redundant neck skin Bilateral microphthalmos Glossoptosis Small earlobe Aplastic clavicle Congenital microcephaly Arrhinencephaly Wide cranial sutures Increased nuchal translucency Short upper lip Severe failure to thrive Inverted nipples Aplasia/Hypoplasia of the middle phalanges of the hand Flared metaphysis Clitoral hypertrophy Abnormality of dental morphology Absent eyebrow Rocker bottom foot Short middle phalanx of finger Metatarsus adductus Aplasia/Hypoplasia of the eyebrow Short clavicles Short finger Absent thumb Abnormality of digit Severe hearing impairment Thin ribs Abnormality of blood and blood-forming tissues Aplasia/Hypoplasia of the thumb Generalized neonatal hypotonia Multiple skeletal anomalies Pyloric stenosis Aplasia of the distal phalanges of the hand Abnormal parietal bone morphology Abnormality of the occipital bone Abnormality of dental structure Aplasia/Hypoplasia of the scapulae Narrow nasal base Aplasia/Hypoplasia of the proximal phalanx of the hallux Aplasia/hypoplasia of the 1st metatarsal Abnormal pelvis bone morphology Aplasia of the distal phalanx of the hallux Dilated cardiomyopathy Atrioventricular block Myocardial fibrosis Left ventricular noncompaction Left ventricular failure Abnormal left ventricle morphology Tapered toe Short proximal phalanx of hallux Hypoplasia of the frontal lobes Gingival recession Renovascular hypertension Renal artery stenosis Aplasia/Hypoplasia of the distal phalanges of the hand Aplasia/Hypoplasia of the nails Hypoplastic facial bones Aplasia/Hypoplasia of the clavicles Abnormality of the scapula Shortening of all distal phalanges of the toes Generalized hypotrichosis Broad secondary alveolar ridge Absent sternal ossification Bilateral external ear deformity Aplasia/Hypoplasia of the hallux Slender long bones with narrow diaphyses Aplasia of the 1st metacarpal Sparse eyebrow Abnormality of the urinary system Pulmonary hypoplasia Prematurely aged appearance Large hands Tricuspid regurgitation Bilateral cryptorchidism Reduced subcutaneous adipose tissue Natal tooth Anteriorly placed anus Hypoplastic nipples Coarse hair Underdeveloped supraorbital ridges Turricephaly Coronal craniosynostosis Premature skin wrinkling Prominent superficial veins Deep palmar crease Venous malformation Aortic aneurysm Abnormality of vision Dermal translucency Oligohydramnios Everted lower lip vermilion Hypoplasia of the maxilla Triangular face Intestinal malrotation Convex nasal ridge Microdontia Low posterior hairline Oligodontia Short palpebral fissure Hypertrichosis Heterotopia Left ventricular hypertrophy Low anterior hairline Generalized hirsutism Scrotal hypoplasia Hypoplasia of the musculature Absence of subcutaneous fat Abnormality of pelvic girdle bone morphology Large fontanelles Single transverse palmar crease Tapered finger Hypopigmentation of the skin Hypodontia Neuronal loss in central nervous system Cardiomegaly Short phalanx of finger Dolichocephaly Short thumb Sparse and thin eyebrow Short toe Short ribs Short chin Sparse eyelashes Tented upper lip vermilion Thin vermilion border Microtia Recurrent aspiration pneumonia Aplasia/Hypoplasia of the nasal bone Upper eyelid coloboma Absent distal phalanges Wide nasal ridge Hypoplasia of the abdominal wall musculature Congenital craniofacial dysostosis Aplastic/hypoplastic lacrimal glands High palate Short philtrum Cardiomyopathy Hypospadias Upslanted palpebral fissure Polyhydramnios Hypertrophic cardiomyopathy Irritability Protruding ear Absent toe Cystathioninemia Absent fingernail Obstructive lung disease Neoplasm Abnormality of nasopharyngeal adenoids Localized skin lesion Dysplastic aortic valve Focal seizures, afebril Intervertebral space narrowing Dermatan sulfate excretion in urine Abnormality of mucopolysaccharide metabolism Short digit Anisopoikilocytosis Urinary glycosaminoglycan excretion Heparan sulfate excretion in urine Morphological abnormality of the central nervous system J-shaped sella turcica Delayed speech and language development Abnormality of the optic disc Hyperplasia of the maxilla Hypochromic anemia Inspiratory stridor Thoracolumbar kyphosis Increased mean corpuscular volume Communicating hydrocephalus Beaking of vertebral bodies Edema of the lower limbs Insomnia Protuberant abdomen Distal arthrogryposis Heart murmur Recurrent upper respiratory tract infections Spasticity Cerebral atrophy Tachypnea Lipodystrophy Eyelid coloboma Skin tags Capillary hemangioma Arachnoid cyst Abnormal eyelash morphology Nevus flammeus Lipoma Hypoplasia of the iris Hamartoma Absent septum pellucidum Multiple lipomas Dysphasia Aphasia Mutism Hydronephrosis Hemangioma Sacral dimple Muscle stiffness Subcutaneous nodule Intellectual disability, profound Cerebral calcification Nevus Tetraplegia Iris coloboma Papule Neurological speech impairment Coloboma Scarring Paralysis Increased intracranial pressure Progressive hearing impairment Ectopia pupillae Abnormality of the clavicle Bruising susceptibility Abnormality of movement Narrow chest Apnea Facial palsy Abnormality of metabolism/homeostasis Enlarged cerebellum Aplasia/Hypoplasia of the mandible Fibular bowing Metaphyseal chondrodysplasia Cloverleaf skull Central apnea Megalencephaly Tibial bowing Recurrent fractures Femoral bowing Mesomelia Thoracic hypoplasia Sleep apnea Acanthosis nigricans Exotropia Rhizomelia Epidermal acanthosis Lumbar hyperlordosis High myopia Generalized-onset seizure Brain atrophy Micromelia Severe short stature Delayed eruption of teeth Abnormal blistering of the skin Thickened skin Opsoclonus Recurrent otitis media Mitral valve prolapse Abnormality of the cardiovascular system Limitation of joint mobility Macroglossia Tachycardia Joint stiffness Developmental regression Coarse facial features Kyphoscoliosis Hyperactivity Prominent forehead Inguinal hernia Short neck Optic nerve compression Abnormality of the ribs Abnormality of temperature regulation Abnormality of hair texture Chronic rhinitis Osteopetrosis Abnormality of visual evoked potentials Reticulocytosis Hypophosphatemia Reduced bone mineral density Cranial nerve paralysis Hypocalcemia Bone marrow hypocellularity Abnormality of epiphysis morphology Bowing of the long bones Abnormality of the metaphysis Dysostosis multiplex Echolalia Absent hand Vitamin B12 deficiency Prominent nasal bridge Abnormality of the kidney EEG abnormality Abnormality of cardiovascular system morphology Dilatation Talipes equinovarus Cognitive impairment Cleft palate Thyroglossal cyst Diffuse hepatic steatosis Decreased methylmalonyl-CoA mutase activity Hypomethioninemia Cystathioninuria Decreased methionine synthase activity Leukemia Decreased adenosylcobalamin Hyperhomocystinemia Decreased methylcobalamin Urogenital fistula Delirium Abnormality of macular pigmentation Chronic hemolytic anemia Methylmalonic acidemia Atrophy of the spinal cord Hemolytic-uremic syndrome Right ventricular failure Gastritis Myelopathy Homocystinuria Finger syndactyly Pulmonic stenosis Cor pulmonale Central hypotonia Aplastic/hypoplastic toenail Chylothorax Aplasia cutis congenita of scalp Periventricular leukomalacia Congenital hepatic fibrosis Esophageal varix Abnormality of the upper limb Pulmonary artery atresia Hypoplastic fingernail Abnormality of the lower limb Arteriovenous malformation Calvarial skull defect Double outlet right ventricle Oligodactyly Talipes Cutaneous finger syndactyly Aplasia/Hypoplasia of the skin Hypoplastic left heart Supernumerary nipple Cutis marmorata Meningitis Telangiectasia Encephalocele Split hand Nail dysplasia Esotropia Gastrointestinal hemorrhage Polymicrogyria Cleft upper lip Methylmalonic aciduria Megaloblastic anemia Hemihypertrophy Tricuspid valve prolapse Weight loss Renal insufficiency Lipomas of the central neryous system Abnormal cartilage morphology Linear hyperpigmentation Osteochondrosis Odontoma Neurodevelopmental abnormality Neoplasm of the skeletal system Pelvic kidney Chorioretinitis Hemiatrophy Subcutaneous lipoma Epibulbar dermoid Reduced visual acuity Abnormal nasolacrimal system morphology Subcortical cerebral atrophy Abnormal anterior chamber morphology Alopecia areata Abnormal aortic morphology Visceral angiomatosis Glioma Interrupted aortic arch Bone cyst Peripheral pulmonary artery stenosis Subvalvular aortic stenosis Craniofacial hyperostosis Astrocytoma Xanthomatosis Gait ataxia Acidosis Thromboembolism Neutropenia Disproportionate tall stature Apathy Ectopia lentis Slurred speech Atherosclerosis Abnormality of retinal pigmentation Anorexia Broad-based gait Psychosis Abnormality of extrapyramidal motor function Pigmentary retinopathy Memory impairment Aciduria Urinary incontinence Metabolic acidosis Arthritis Hepatic steatosis Nephropathy Hemolytic anemia Joint hypermobility Long face Abnormality of skin pigmentation Retinal degeneration Paresthesia Unsteady gait Confusion Lower limb muscle weakness Congenital cataract Lethargy Feeding difficulties in infancy Left ventricular noncompaction cardiomyopathy


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