Intrauterine growth retardation, and Aortic valve stenosis

Diseases related with Intrauterine growth retardation and Aortic valve stenosis

In the following list you will find some of the most common rare diseases related to Intrauterine growth retardation and Aortic valve stenosis that can help you solving undiagnosed cases.

Top matches:

RENAL-HEPATIC-PANCREATIC DYSPLASIA 1; RHPD1 Is also known as rhpd

Related symptoms:

  • Growth delay
  • Hypertelorism
  • Flexion contracture
  • Hepatomegaly
  • Intrauterine growth retardation


SOURCES: OMIM MENDELIAN

More info about RENAL-HEPATIC-PANCREATIC DYSPLASIA 1; RHPD1

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

High match ROBERTS SYNDROME

Roberts syndrome (RBS) is characterized by pre- and postnatal growth retardation, severe symmetric limb reduction defects, craniofacial anomalies and severe intellectual deficit. SC phocomelia is a milder form of RBS.

ROBERTS SYNDROME Is also known as pseudothalidomide syndrome|roberts-sc phocomelia syndrome|sc pseudothalidomide syndrome|sc phocomelia

Related symptoms:

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


SOURCES: OMIM ORPHANET MENDELIAN

More info about ROBERTS SYNDROME

Other less relevant matches:

High match 3C SYNDROME

Cranio-cerebello-cardiac (3C) syndrome is a rare multiple congenital anomalies syndrome characterized by craniofacial (prominent occiput and forehead, hypertelorism, ocular coloboma, cleft palate), cerebellar (Dandy-Walker malformation, cerebellar vermis hypoplasia) and cardiac (tetralogy of Fallot, atrial and ventricular septal defects) anomalies (see these terms).

3C SYNDROME Is also known as dandy-walker-like malformation with atrioventricular septal defect|craniocerebellocardiac dysplasia|3c syndrome|ritscher-schinzel syndrome

Related symptoms:

  • Intellectual disability
  • Global developmental delay
  • Short stature
  • Generalized hypotonia
  • Microcephaly


SOURCES: ORPHANET OMIM MENDELIAN

More info about 3C SYNDROME

High match MYHRE SYNDROME

Myhre syndrome is characterised by striking muscular build, short stature, reduced joint mobility, brachydactyly, mixed hearing loss and mental retardation of variable severity. Facial dysmorphism with short palpebral fissures, short philtrum, thin lips, maxillary hypoplasia and prognathism is present. Thick skin has been observed in six patients.

MYHRE SYNDROME Is also known as laryngotracheal stenosis, arthropathy, prognathism, and short stature|laps syndrome|growth-mental deficiency syndrome of myhre|facial dysmorphism-intellectual disability-short stature-hearing loss syndrome

Related symptoms:

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


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about MYHRE SYNDROME

Prader-Willi syndrome is characterized by diminished fetal activity, obesity, muscular hypotonia, mental retardation, short stature, hypogonadotropic hypogonadism, and small hands and feet. It can be considered to be an autosomal dominant disorder and is caused by deletion or disruption of a gene or several genes on the proximal long arm of the paternal chromosome 15 or maternal uniparental disomy 15, because the gene(s) on the maternal chromosome(s) 15 are virtually inactive through imprinting. Horsthemke and Wagstaff (2008) provided a detailed review of the mechanisms of imprinting of the Prader-Willi/Angelman syndrome (OMIM ) region.See also the chromosome 15q11-q13 duplication syndrome (OMIM ), which shows overlapping clinical features.

PRADER-WILLI SYNDROME; PWS Is also known as prader-labhart-willi syndrome

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Generalized hypotonia


SOURCES: OMIM MENDELIAN

More info about PRADER-WILLI SYNDROME; PWS

Medium match JACOBSEN SYNDROME

Jacobsen syndrome is a multiple congenital anomaly/mental retardation (MCA/MR) contiguous gene syndrome caused by partial deletion of the long arm of chromosome 11.

JACOBSEN SYNDROME Is also known as monosomy 11qter|del(11)(q23.3)|distal deletion 11q|telomeric deletion 11q|distal monosomy 11q|del(11)(qter)|chromosome 11q deletion syndrome|partial 11q monosomy syndrome

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Generalized hypotonia


SOURCES: OMIM ORPHANET MENDELIAN

More info about JACOBSEN SYNDROME

Medium match WILLIAMS SYNDROME

Williams syndrome is a rare genetic multisystemic neurodevelopmental disorder characterized by a distinct facial appearance, cardiac anomalies (most frequently supravalvular aortic stenosis), cognitive and developmental abnormalities, and connective tissue abnormalities (such as joint laxity)

WILLIAMS SYNDROME Is also known as deletion 7q11.23|williams syndrome|williams-beuren syndrome|chromosome 7q11.23 deletion syndrome, 1.5- to 1.8-mb|wms|monosomy 7q11.23|ws

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Generalized hypotonia


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about WILLIAMS SYNDROME

Autosomal dominant cutis laxa-3 is characterized by thin skin with visible veins and wrinkles, cataract or corneal clouding, clenched fingers, pre- and postnatal growth retardation, and moderate intellectual disability. In addition, patients exhibit a combination of muscular hypotonia with brisk muscle reflexes (Fischer-Zirnsak et al., 2015).For a general phenotypic description and discussion of genetic heterogeneity of autosomal dominant cutis laxa, see ARCL1 (OMIM ).

Related symptoms:

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


SOURCES: OMIM MENDELIAN

More info about CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3

This syndrome is characterised by the association of toe syndactyly, facial dysmorphism including telecanthus (abnormal distance between the eyes) and a broad nasal tip, urogenital malformations and anal atresia.

SYNDACTYLY-TELECANTHUS-ANOGENITAL AND RENAL MALFORMATIONS SYNDROME Is also known as star syndrome|syndactyly with renal and anogenital malformations

Related symptoms:

  • Seizures
  • Short stature
  • Hearing impairment
  • Abnormal facial shape
  • Low-set ears


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about SYNDACTYLY-TELECANTHUS-ANOGENITAL AND RENAL MALFORMATIONS SYNDROME

Top 5 symptoms//phenotypes associated to Intrauterine growth retardation and Aortic valve stenosis

Symptoms // Phenotype % cases
Growth delay Very Common - Between 80% and 100% cases
Global developmental delay Common - Between 50% and 80% cases
Intellectual disability Common - Between 50% and 80% cases
Short stature Common - Between 50% and 80% cases
Microcephaly Common - Between 50% and 80% cases

Other less frequent symptoms

Patients with Intrauterine growth retardation and Aortic valve stenosis. may also develop some of the following symptoms:

Common Symptoms - More than 50% cases

Seizures

Uncommon Symptoms - Between 30% and 50% cases

Abnormal cardiac septum morphology

Common Symptoms - More than 50% cases

Syndactyly

Uncommon Symptoms - Between 30% and 50% cases

Ventricular septal defect

Common Symptoms - More than 50% cases

Cataract

Uncommon Symptoms - Between 30% and 50% cases

Muscular hypotonia

Common Symptoms - More than 50% cases

Strabismus

Uncommon Symptoms - Between 30% and 50% cases

Generalized hypotonia

Common Symptoms - More than 50% cases

Abnormal facial shape

Uncommon Symptoms - Between 30% and 50% cases

Patent ductus arteriosus

Common Symptoms - More than 50% cases

Abnormal heart morphology

Uncommon Symptoms - Between 30% and 50% cases

Flexion contracture Scoliosis Recurrent respiratory infections Postnatal growth retardation Cleft palate Atrial septal defect Brachydactyly Short neck Abnormality of cardiovascular system morphology Cryptorchidism Micrognathia Osteopenia Inguinal hernia Low-set ears Feeding difficulties Hypertelorism Macrocephaly Finger syndactyly Talipes equinovarus Coarctation of aorta Hypertension Small for gestational age Abnormality of the skeletal system Intellectual disability, mild Congestive heart failure Ventriculomegaly Prominent nasal bridge Microphthalmia Dilatation Thin upper lip vermilion Autism Toe syndactyly Behavioral abnormality Sparse hair Failure to thrive Bicuspid aortic valve Clinodactyly of the 5th finger Hearing impairment Depressed nasal bridge Wide nasal bridge Short nose Abnormality of the kidney Prominent forehead Clinodactyly Craniosynostosis Horseshoe kidney Frontal bossing Hypospadias Obesity Constipation Hypogonadism Kyphosis Autistic behavior Malar flattening Chronic constipation Double outlet right ventricle Pulmonary artery stenosis Abnormality of the cardiovascular system Glaucoma Hypoplastic left heart Delayed speech and language development Corneal opacity High forehead Renal agenesis Anal atresia Wormian bones Growth hormone deficiency Postural instability Oral cleft Downslanted palpebral fissures Sensorineural hearing impairment Neurological speech impairment Hydronephrosis Radial deviation of finger Broad forehead Feeding difficulties in infancy Pain Unilateral renal agenesis Cleft lip Ptosis Camptodactyly Precocious puberty Diabetes mellitus Myopia Talipes Hernia Infantile muscular hypotonia Osteoporosis Abnormality of the dentition Premature birth Cerebellar hypoplasia Thrombocytopenia Hydrocephalus Spontaneous abortion Attention deficit hyperactivity disorder Leukemia Esotropia Pulmonic stenosis Tetralogy of Fallot Hemiparesis Renal insufficiency Oligohydramnios Epicanthus Intestinal malrotation Polymicrogyria Cognitive impairment

Rare Symptoms - Less than 30% cases

Narrow nasal bridge Eyelid coloboma Bifid uvula Atrioventricular canal defect Spasticity Chorioretinal coloboma Carious teeth Full cheeks Hand polydactyly Sleep disturbance Labial hypoplasia Hemivertebrae Genu valgum Hypoplasia of penis Coloboma Iris coloboma Abnormality of lipid metabolism Hip dislocation Clitoral hypoplasia Smooth philtrum Single transverse palmar crease Optic atrophy Otitis media Microdontia Immunodeficiency Dehydration Abnormal form of the vertebral bodies Narrow forehead Amblyopia Gastroesophageal reflux Spina bifida Glucose intolerance Schizophrenia Failure to thrive in infancy Dolichocephaly Hypogonadotrophic hypogonadism Increased body weight Type II diabetes mellitus Posterior embryotoxon Joint laxity Stroke Narrow palpebral fissure Blepharophimosis Scarring Myopathy Hypermetropia Short palm Amenorrhea Specific learning disability Short toe Low-set, posteriorly rotated ears Respiratory tract infection Abnormality of the voice Vesicoureteral reflux Skeletal muscle hypertrophy Broad nasal tip External genital hypoplasia High hypermetropia Protruding ear Wheezing Oligomenorrhea Joint stiffness Narrow mouth Missing ribs Abnormality of the pinna Telecanthus Ectopic anus Mitral stenosis Adducted thumb Pes planus Hypothyroidism Ataxia Peptic ulcer Pectus excavatum Urethral stenosis Respiratory failure Hypoglycemia Motor delay Respiratory distress Cutis laxa Recurrent infections Midface retrusion Spina bifida occulta Micropenis Hyperactivity Intellectual disability, moderate Decreased antibody level in blood Long philtrum Gastrointestinal hemorrhage Radioulnar synostosis Hypoplasia of the radius Small nail Central hypotonia Polycystic kidney dysplasia Short thumb Myocardial infarction Hypoplastic fingernail Pelvic kidney Abnormality of the upper limb Peripheral pulmonary artery stenosis Chest pain Cleft upper lip Paralysis Retrognathia Alopecia Aortic regurgitation Hypertonia Brachycephaly High palate Neoplasm Clitoral hypertrophy Nystagmus Subvalvular aortic stenosis Respiratory insufficiency Cirrhosis Pachygyria Portal hypertension Facial hemangioma Dandy-Walker malformation Nasolacrimal duct obstruction Early onset of sexual maturation Irritability Abnormality of the anus Overfriendliness Toe clinodactyly Abnormal carotid artery morphology Abnormality of the diencephalon Giant platelets Macular hypoplasia Central hypothyroidism Vocal cord dysfunction U-Shaped upper lip vermilion Developmental regression Nystagmus-induced head nodding Hyperlordosis Dyssynergia Stellate iris Functional abnormality of male internal genitalia Long hallux Descending aorta hypoplasia Abnormality of the head Abdominal pain Annular pancreas Hypertrophic cardiomyopathy Hyperreflexia Delayed skeletal maturation Depressivity Cerebral cortical atrophy Macrotia Kyphoscoliosis Absent speech Gait disturbance Tremor Arthralgia Elfin facies Coarse facial features Dysarthria Visual impairment Elevated serum creatine phosphokinase Broad columella Megakaryocyte dysplasia Congenital thrombocytopenia Umbilical hernia Bilateral vocal cord paralysis Thyroid hemiagenesis Bilateral camptodactyly Anxiety Proteinuria Arteria lusoria Medial flaring of the eyebrow Internal hemorrhage Abnormality of the curvature of the vertebral column Duodenal atresia Abnormal thrombocyte morphology Macular dystrophy Multicystic kidney dysplasia Bone marrow hypocellularity Leukodystrophy Sinusitis Small foramen magnum Bulbous nose Pancytopenia Wide nose Eczema Retinal dystrophy Ectopic kidney Webbed neck Microcornea Bruising susceptibility Azoospermia Tachycardia Anal stenosis Facial asymmetry Syringomyelia Narrow chest Narrow nose Skin rash Rectovaginal fistula Bicornuate uterus Duane anomaly Lop ear Agenesis of corpus callosum 4-5 toe syndactyly Cerebral atrophy Holoprosencephaly Abnormal palate morphology Atrophy/Degeneration involving the corticospinal tracts Natal tooth Aplasia/Hypoplasia of the earlobes Nuclear cataract Congenital cataract Broad hallux phalanx Wide mouth Triangular face Thin skin Retinal dysplasia Diastasis recti Brisk reflexes Abnormal eyelash morphology Bipolar affective disorder Transposition of the great arteries Slender finger Tachypnea Partial agenesis of the corpus callosum Delayed cranial suture closure Reduced subcutaneous adipose tissue Aplasia/Hypoplasia of the eyebrow Flat occiput Spinal canal stenosis Hammertoe Heart murmur Premature skin wrinkling Ectropion Trigonocephaly Pyloric stenosis Calcaneovalgus deformity Dermal translucency Paroxysmal bursts of laughter Arnold-Chiari type I malformation Nausea and vomiting Obsessive-compulsive behavior Celiac disease Vertebral segmentation defect Premature graying of hair Hallux valgus Arterial stenosis Open bite Loss of consciousness Dysgraphia Polyuria Abnormality of nervous system morphology Tracheoesophageal fistula Hypoplastic toenails Abnormality of dental morphology Chronic otitis media Prematurely aged appearance Phonophobia Parathyroid hyperplasia Nephritis Hypercalcemia Redundant skin Cholelithiasis Hypercalciuria Abnormal glucose tolerance Dysphonia Polycystic ovaries Incoordination Abnormality of pelvic girdle bone morphology Increased nuchal translucency Reduced bone mineral density Rectal prolapse Periorbital edema Ischemic stroke Large earlobe Insomnia Nevus flammeus Soft skin Poor coordination Abnormality of the vasculature Patellar dislocation Multiple renal cysts Down-sloping shoulders Vocal cord paralysis Blue irides Hypoplasia of the zygomatic bone Right ventricular hypertrophy Tubulointerstitial nephritis Abnormality of the neck Cystic renal dysplasia Abnormality of the cerebral vasculature Enuresis Villous atrophy Restlessness Dyslexia Cerebral ischemia Abnormality of refraction Gait imbalance Periorbital fullness Decreased plasma carnitine Facial cleft Abnormal renal morphology Lacrimation abnormality Bladder diverticulum Arnold-Chiari malformation Sacral dimple Malabsorption Hypotelorism Mitral regurgitation Open mouth Infantile hypercalcemia Abnormality of the gastric mucosa Recurrent otitis media Thick lower lip vermilion Renal hypoplasia Ventricular hypertrophy Hypsarrhythmia Cardiomegaly Abnormality of extrapyramidal motor function Mitral valve prolapse Renovascular hypertension Abnormal social behavior Food intolerance Dental malocclusion Flat cornea Supravalvular aortic stenosis Impaired visuospatial constructive cognition Sudden cardiac death Macroglossia Megalocornea Unilateral renal hypoplasia Hypodontia Everted lower lip vermilion Thick vermilion border Dysmetria Joint hyperflexibility Myxomatous mitral valve degeneration Involuntary movements Recurrent urinary tract infections Widely spaced teeth Obsessive-compulsive trait Progressive hearing impairment Retinal vascular tortuosity Thyroid hypoplasia Abnormal dermatoglyphics Abnormal endocardium morphology Aplasia/Hypoplasia of the iris Renal duplication Colonic diverticula Vascular tortuosity Abnormality of the ankles Tubulointerstitial abnormality Overriding aorta Aortic arch aneurysm Nocturia Nephrolithiasis Synostosis of joints Abnormality of the fingernails Abnormality of the bladder Abnormality of dental enamel Nephrocalcinosis Renal artery stenosis Coronary artery stenosis Retinal arteriolar tortuosity Hyperacusis Pointed chin Increased bone mineral density Narrow face Hoarse voice Gingival overgrowth Calcification of the aorta Constrictive pericarditis Anteverted nares Absent thumb Phocomelia Long penis Patellar aplasia Fair hair Low hanging columella Capillary hemangioma Upper limb undergrowth Severe intrauterine growth retardation External ear malformation Synostosis of carpal bones Underdeveloped supraorbital ridges Absent radius Hip contracture Aplasia/Hypoplasia of the thumb Short femoral neck Wrist flexion contracture Blue sclerae Posteriorly rotated ears Proptosis Polyhydramnios Hypotrichosis Falls Underdeveloped nasal alae Bowing of the long bones Proximal placement of thumb Bilateral single transverse palmar creases Knee flexion contracture Opacification of the corneal stroma Sandal gap Hemangioma Melanoma Humeroradial synostosis Aplasia of the ulna Aplasia cutis congenita over posterior parietal area Enlarged cisterna magna Mesomelia Congenital glaucoma Abnormality of the hip bone Adrenal hypoplasia Pierre-Robin sequence Single umbilical artery Communicating hydrocephalus Abnormality of neuronal migration Abnormal mitral valve morphology Aplasia/Hypoplasia of the nipples Complete atrioventricular canal defect Lethal skeletal dysplasia Abnormal tricuspid valve morphology Abnormality of the fontanelles or cranial sutures Prominent occiput Aplasia/Hypoplasia of the cerebellum Complete duplication of thumb phalanx Skeletal dysplasia Absent earlobe Progressive flexion contractures Mesomelic arm shortening Tetraphocomelia Midface capillary hemangioma Premature separation of centromeric heterochromatin High, narrow palate Abnormality of the hand Limb undergrowth Low posterior hairline Cerebellar vermis hypoplasia Large fontanelles Preauricular skin tag Narrow palate Aplasia cutis congenita on trunk or limbs Acrania Contractures of the large joints Polysplenia Hypoplasia of the corpus callosum Pancreatic dysplasia Ureteral atresia Multiple glomerular cysts Glutaric acidemia Pancreatic fibrosis Potter facies Portal fibrosis Hepatic cysts Pancreatic cysts Short sternum Bile duct proliferation Biliary cirrhosis Asplenia Enlarged kidney Short distal phalanx of finger Pulmonary hypoplasia Hepatomegaly Polydactyly Acidosis Jaundice Stage 5 chronic kidney disease Hepatic failure Postaxial polydactyly Preauricular pit Renal cyst Cholestasis Renal dysplasia Hepatic fibrosis Situs inversus totalis Type I diabetes mellitus EEG abnormality Ascites Imperforate hymen Aplastic/hypoplastic toenail Esophageal varix Congenital hepatic fibrosis Porencephalic cyst Periventricular leukomalacia Aplasia cutis congenita of scalp Chylothorax Absent hand Abnormality of the lower limb Absent fingernail Venous malformation Abnormal pulmonary valve morphology Absent toe Cutis marmorata telangiectatica congenita Periventricular cysts Pulmonary artery atresia Arteriovenous malformation Nail dysplasia Abnormality of the metacarpal bones Pulmonary arterial hypertension Split hand Encephalocele Telangiectasia Meningitis Leukopenia Cutis marmorata Calvarial skull defect Supernumerary nipple Cortical dysplasia Aplasia/Hypoplasia of the skin Cutaneous finger syndactyly Aplasia cutis congenita Oligodactyly Posterior fossa cyst Humoral immunodeficiency Acromicria Hip dysplasia Large hands Emotional lability Hyperinsulinemia Nasal speech Poor suck Scrotal hypoplasia Sleep apnea Bradycardia Insulin resistance Clumsiness Primary amenorrhea Cutaneous photosensitivity Psychosis Decreased fetal movement Febrile seizures Albinism Delayed puberty Weight loss Photophobia Neonatal hypotonia Abnormality of the nervous system Apnea Pruritus Infertility Sepsis Arachnodactyly Downturned corners of mouth Small hand Short foot Tapered finger Hypopigmentation of the skin Inflammation of the large intestine Adrenal insufficiency Hyporeflexia Temperature instability Poor fine motor coordination Anteverted ears Frontal upsweep of hair Erysipelas Disseminated intravascular coagulation Triangular mouth Central adrenal insufficiency Cor pulmonale Hypoplastic labia minora Psychotic episodes Narrow palm Hypopnea Almond-shaped palpebral fissure Poor gross motor coordination Abdominal obesity Generalized hypopigmentation Decreased muscle mass Hypopigmentation of hair Truncal obesity Polyphagia Myeloid leukemia Impaired pain sensation Striae distensae Pulmonary embolism Hypoventilation Hypothermia Iris hypopigmentation Overweight Acrocyanosis Hypoplasia of the fovea Chromosome breakage Ocular albinism Upslanted palpebral fissure Vomiting Cerebellar malformation Abnormality of epiphysis morphology Fine hair Short palpebral fissure Choanal atresia Abnormal lung morphology Abnormality of the metaphysis Thickened skin EMG abnormality Limitation of joint mobility Short long bone Cone-shaped epiphysis Stridor Oral-pharyngeal dysphagia Overlapping toe 2-3 toe syndactyly Abnormality of the ribs Progressive cerebellar ataxia Pericardial effusion Conductive hearing impairment Primum atrial septal defect Cardiomyopathy Cerebellar atrophy Severe short stature Mandibular prognathia Deeply set eye Microtia Hypoplasia of the maxilla Cough Short philtrum Platyspondyly Astigmatism Thin vermilion border Thick eyebrow Blurred vision Short finger Intellectual disability, severe Abnormality of the pubic bone Abnormality of the penis Stiff skin Pseudopapilledema Esophageal stenosis Large iliac wings Pear-shaped nose Generalized muscle hypertrophy Unilateral cleft lip Laryngotracheal stenosis Enlarged vertebral pedicles Gingival cleft Hypoplasia of eyelid Fever Edema Abnormal lip morphology Abnormality of the menstrual cycle Vertebral fusion Irregular vertebral endplates Abnormal joint morphology Thickened calvaria Keratoconus Arthropathy Pericarditis Submucous cleft hard palate Hypoplastic iliac wing Epispadias Tracheal stenosis Broad ribs Restrictive cardiomyopathy Craniofacial hyperostosis Constrictive median neuropathy Femoral hernia Mitral atresia


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