Myopathy, and Aortic valve stenosis

Diseases related with Myopathy and Aortic valve stenosis

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

Top matches:

Noonan syndrome-like disorder with juvenile myelomonocytic leukemia is a rare, genetic, polymalformative syndrome with increased risk of developing cancer characterized by a Noonan-like phenotype, including typical dysmorphic facial features (i.e. high forehead, hypertelorism, downslanting palpebral fissures, ptosis, low-set ears, prominent philtrum and short neck with or without pterygium colli), thoracic abnormalities, congenital heart defects and short stature, associated with a very frequent ocurrence of juvenile myelomonocytic leukemia. Developmental delay, ectodermal anomalies, joint laxity, and hypotonia may also be associated.

NOONAN SYNDROME-LIKE DISORDER WITH JUVENILE MYELOMONOCYTIC LEUKEMIA Is also known as cbl mutation-associated syndrome|noonan syndrome-like disorder with jmml|cbl syndrome

Related symptoms:

  • Global developmental delay
  • Short stature
  • Generalized hypotonia
  • Microcephaly
  • Growth delay


SOURCES: ORPHANET OMIM MENDELIAN

More info about NOONAN SYNDROME-LIKE DISORDER WITH JUVENILE MYELOMONOCYTIC LEUKEMIA

Osteopathia striata with cranial sclerosis (OS-CS) is a bone dysplasia characterized by longitudinal striations of the metaphyses of the long bones, sclerosis of the craniofacial bones, macrocephaly, cleft palate and hearing loss.

OSTEOPATHIA STRIATA-CRANIAL SCLEROSIS SYNDROME Is also known as hyperostosis generalisata with striations|robinow-unger syndrome

Related symptoms:

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


SOURCES: ORPHANET MESH OMIM MENDELIAN

More info about OSTEOPATHIA STRIATA-CRANIAL SCLEROSIS 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

Other less relevant matches:

CHANARIN-DORFMAN SYNDROME; CDS Is also known as neutral lipid storage disease with ichthyosis|dcs|nlsdi|triglyceride storage disease with impaired long-chain fatty acid oxidation|dorfman-chanarin syndrome|chanarin-dorfman disease|ichthyosiform erythroderma with leukocyte vacuolation|ichthyotic neutral

Related symptoms:

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


SOURCES: OMIM ORPHANET MENDELIAN

More info about CHANARIN-DORFMAN SYNDROME; CDS

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

Multiple pterygium syndromes comprise a group of multiple congenital anomaly disorders characterized by webbing (pterygia) of the neck, elbows, and/or knees and joint contractures (arthrogryposis) (Morgan et al., 2006). The multiple pterygium syndromes are phenotypically and genetically heterogeneous but are traditionally divided into prenatally lethal (OMIM ) and nonlethal (Escobar) types.

MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS Is also known as escobar syndrome|multiple pterygium syndrome|pterygium syndrome|multiple pterygium syndrome, nonlethal type|pterygium colli syndrome|pterygium universale

Related symptoms:

  • Short stature
  • Hearing impairment
  • Scoliosis
  • Hypertelorism
  • Micrognathia


SOURCES: OMIM MENDELIAN

More info about MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS

Ehlers-Danlos syndrome, kyphoscoliotic type (EDKT) is a form of Ehlers-Danlos syndrome characterized by severe hypotonia and kyphoscoliosis at birth, generalized joint hyperextensibility and ocular globe fragility.

EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE Is also known as eds vi|eds6|ehlers-danlos syndrome, oculoscoliotic type|ehlers-danlos syndrome, ocular-scoliotic type|eds, oculoscoliotic type|eds6a, formerly|nevo syndrome|eds via|ehlers-danlos syndrome, type vi|ehlers-danlos syndrome, type via, formerly|eds, kyphoscoli

Related symptoms:

  • Generalized hypotonia
  • Scoliosis
  • Muscle weakness
  • Muscular hypotonia
  • Cryptorchidism


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE

Medium match MARFAN SYNDROME; MFS

A heritable disorder of fibrous connective tissue, Marfan syndrome shows striking pleiotropism and clinical variability. The cardinal features occur in 3 systems--skeletal, ocular, and cardiovascular (McKusick, 1972; Pyeritz and McKusick, 1979; Pyeritz, 1993). It shares overlapping features with congenital contractural arachnodactyly (OMIM ), which is caused by mutation in the FBN2 gene (OMIM ).Gray and Davies (1996) gave a general review. They published Kaplan-Meier survival curves for a cohort of British Marfan syndrome patients demonstrating greater survivorship in females than in males; a similar result had been reported by Murdoch et al. (1972) and by Silverman et al. (1995). Gray and Davies (1996) also proposed a grading scale for clinical comparison of the Marfan syndrome patients. The authors provided criteria for each grade and suggested uniform use of these scales may facilitate clinicomolecular correlations.

MARFAN SYNDROME; MFS Is also known as marfan syndrome, type i|mfs1

Related symptoms:

  • Intellectual disability
  • Generalized hypotonia
  • Scoliosis
  • Micrognathia
  • Strabismus


SOURCES: OMIM MENDELIAN

More info about MARFAN SYNDROME; MFS

Related symptoms:

  • Muscle weakness
  • Ventriculomegaly
  • Cardiomyopathy
  • Myopathy
  • Congestive heart failure


SOURCES: OMIM MESH MENDELIAN

More info about CARDIOMYOPATHY, DILATED, 1S; CMD1S

A well differentiated, low grade neuroendocrine tumor (carcinoid tumor) that arises from the small or large intestine. The mitotic count is less than 2 per 10 HPF and/or the Ki67 index is equal to or less than 2 percent.

CARCINOID SYNDROME Is also known as malignant carcinoid syndrome

Related symptoms:

  • Neoplasm
  • Myopathy
  • Elevated hepatic transaminase
  • Nausea and vomiting
  • Asthma


SOURCES: OMIM ORPHANET MENDELIAN

More info about CARCINOID SYNDROME

Top 5 symptoms//phenotypes associated to Myopathy and Aortic valve stenosis

Symptoms // Phenotype % cases
Generalized hypotonia Common - Between 50% and 80% cases
Pectus excavatum Common - Between 50% and 80% cases
Epicanthus Common - Between 50% and 80% cases
Short stature Common - Between 50% and 80% cases
Scoliosis Common - Between 50% and 80% cases

Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases

Global developmental delay Intellectual disability Congestive heart failure Flexion contracture Arachnodactyly Micrognathia Dilatation Depressed nasal bridge Kyphosis Abnormal facial shape Strabismus Esotropia Cryptorchidism Ptosis Stroke Pain Cataract Hearing impairment High palate Joint laxity Talipes equinovarus Gastroesophageal reflux Prominent forehead Aortic regurgitation Muscle weakness Bicuspid aortic valve Hernia Inguinal hernia Long philtrum Hyperlordosis Dental malocclusion Failure to thrive Muscular hypotonia Low-set ears Cognitive impairment Delayed speech and language development Dolichocephaly Downslanted palpebral fissures Edema Respiratory distress Myopia Camptodactyly Intellectual disability, mild Coarctation of aorta Failure to thrive in infancy Oligohydramnios Increased body weight Dental crowding Respiratory insufficiency Decreased muscle mass Decreased fetal movement Abnormality of the cardiovascular system Syndactyly Osteopenia Osteoporosis Micropenis Spontaneous abortion Seizures Long face Clinodactyly Spina bifida occulta Cleft palate Abnormality of the dentition Ventriculomegaly Heart murmur Apnea Abnormality of the skeletal system Neoplasm Narrow forehead Thick vermilion border Motor delay Short neck Glaucoma Atrial septal defect Gait disturbance Kyphoscoliosis Joint hypermobility Abnormality of cardiovascular system morphology Pes planus Pulmonic stenosis Macrocephaly Hypertension Mitral regurgitation Broad forehead Pectus carinatum Mitral valve prolapse Hypertelorism Growth delay Feeding difficulties High forehead

Rare Symptoms - Less than 30% cases

Ventricular hypertrophy Obesity Overgrowth Intrauterine growth retardation Pulmonary artery stenosis Short nose Behavioral abnormality Cardiomegaly Soft skin Clitoral hypoplasia Slender finger Nystagmus Nasal speech Open bite Thick lower lip vermilion Open mouth Abnormal vertebral morphology Joint contracture of the hand Increased bone mineral density Spina bifida Narrow palate Cutaneous syndactyly Narrow face Tall stature Epiphora Dural ectasia Aortic dissection Amblyopia Megalocornea Aortic root aneurysm Down-sloping shoulders Disproportionate tall stature Redundant skin Recurrent respiratory infections Nausea and vomiting Chest pain Flat cornea Aortic arch aneurysm Visual impairment Type II diabetes mellitus Decreased plasma carnitine Insulin resistance Everted lower lip vermilion Hypogonadotrophic hypogonadism Sleep apnea Precocious puberty Full cheeks Sensorineural hearing impairment Glucose intolerance Rocker bottom foot Congenital contracture Ataxia Striae distensae Pulmonary embolism Talipes Abnormality of lipid metabolism Gastrointestinal hemorrhage Sepsis Abnormality of the neck Retinal detachment Joint hyperflexibility Hypogonadism Hypopnea Bladder diverticulum Abnormality of the kidney Hypertrophic cardiomyopathy Umbilical hernia Diabetes mellitus Polyneuropathy Autism Sleep disturbance Narrow mouth Neonatal hypotonia Respiratory tract infection Attention deficit hyperactivity disorder Malar flattening Carious teeth Delayed puberty Genu valgum Downturned corners of mouth Infantile muscular hypotonia Aortic aneurysm Macrotia Bruising susceptibility Patent ductus arteriosus Abnormal heart morphology Microtia Craniosynostosis Clinodactyly of the 5th finger Frontal bossing Cleft lip Polyhydramnios Anteverted nares Hypothyroidism Tricuspid regurgitation Posteriorly rotated ears Cardiomyopathy Abnormal bleeding Retrognathia Cholelithiasis Intellectual disability, severe Webbed neck Wide nasal bridge Specific learning disability Feeding difficulties in infancy Conductive hearing impairment Paralysis Low-set, posteriorly rotated ears Wide intermamillary distance Torticollis Broad nasal tip Leukemia Hepatosplenomegaly High, narrow palate Ventricular septal defect Hypermetropia Hip dysplasia Poor suck Microcephaly Overfolded helix Thoracic kyphosis Synostosis of joints Abnormality of the bladder Tubulointerstitial abnormality Nocturia Obsessive-compulsive trait Chronic noninfectious lymphadenopathy Increased serum serotonin Overriding aorta Abnormality of the ankles Protracted diarrhea Vascular tortuosity Colonic diverticula Facial telangiectasia Renal duplication Aplasia/Hypoplasia of the iris Abnormal endocardium morphology Thyroid hypoplasia Retinal vascular tortuosity Renal artery stenosis Infantile hypercalcemia Coronary artery stenosis Overfriendliness Medial flaring of the eyebrow Elfin facies Bilateral vocal cord paralysis Thyroid hemiagenesis Neoplasm of the endocrine system Nystagmus-induced head nodding Early onset of sexual maturation Abnormal carotid artery morphology Dyssynergia Stellate iris Functional abnormality of male internal genitalia Descending aorta hypoplasia Vocal cord dysfunction Atrophy/Degeneration involving the corticospinal tracts Abnormality of the diencephalon Paroxysmal bursts of laughter Retinal arteriolar tortuosity Right ventricular failure Hyperacusis Pelvic kidney Food intolerance Abnormality of the gastric mucosa Renovascular hypertension Abnormal social behavior Rhinorrhea Myxomatous mitral valve degeneration Paraganglioma Carcinoid tumor Supravalvular aortic stenosis Impaired visuospatial constructive cognition Calcification of the aorta Night sweats Unilateral renal hypoplasia Increased nuchal translucency Arterial stenosis Abnormal glucose tolerance Celiac disease Patellar dislocation Abnormality of the vasculature Intestinal carcinoid Erythematous plaque Poor coordination Nevus flammeus Arnold-Chiari type I malformation Posterior embryotoxon Insomnia Restlessness Facial cleft Prematurely aged appearance Small intestine carcinoid High hypermetropia Vertebral segmentation defect Vocal cord paralysis Premature graying of hair Hallux valgus Loss of consciousness Polyuria Tracheoesophageal fistula Hypoplastic toenails Abnormality of dental morphology Unilateral renal agenesis Obsessive-compulsive behavior Chronic otitis media Nephritis Abnormality of the voice Portal hypertension Radioulnar synostosis Multiple renal cysts Blue irides Bronchospasm Abnormal renal morphology Urethral stenosis Parathyroid hyperplasia Lack of bowel sounds Hepatic necrosis Phonophobia Abnormality of nervous system morphology Dysgraphia Episodic abdominal pain Rectal prolapse Periorbital edema Peptic ulcer Cystic renal dysplasia Atypical pulmonary carcinoid tumor Lacrimation abnormality Subvalvular aortic stenosis Hypoplasia of the zygomatic bone Peripheral pulmonary artery stenosis Periorbital fullness Gait imbalance Pulmonary carcinoid tumor Abnormality of refraction Cerebral ischemia Dyslexia Villous atrophy Enuresis Abnormality of the cerebral vasculature Large earlobe Tubulointerstitial nephritis Right ventricular hypertrophy Chronic constipation Skeletal muscle atrophy Pterygium Hypospadias Abnormality of the hip bone Decreased pulmonary function Moderate myopia Wrist drop Premature rupture of membranes Palmoplantar cutis laxa Arterial dissection Keloids Thoracic kyphoscoliosis Lens luxation Subcutaneous hemorrhage Generalized joint laxity Atypical scarring of skin Thoracic aortic aneurysm Keratoconus Atrophic scars Molluscoid pseudotumors Thin skin Hypertropia Generalized muscle weakness Premature osteoarthritis Protrusio acetabuli High myopia Blue sclerae Recurrent pneumonia Endocarditis Hyperbilirubinemia Joint dislocation Corneal dystrophy Hyperextensible skin Intracranial hemorrhage Tricuspid valve prolapse Arterial rupture Spontaneous rupture of the globe Microcornea Low back pain Hypoplasia of the musculature Reduced subcutaneous adipose tissue Abnormality of the sternum Pneumothorax Homocystinuria Dilatation of the cerebral artery Pulmonary edema Ascending tubular aorta aneurysm Spondylolisthesis Subarachnoid hemorrhage Hypoplasia of the iris Arachnoid cyst Meningocele Genu recurvatum Restrictive ventilatory defect Emphysema Progressive congenital scoliosis Abnormal lung morphology Peripheral neuropathy Visual loss Arrhythmia Pes cavus Deeply set eye Peripheral axonal neuropathy Decreased body weight Overbite Exotropia Elbow flexion contracture Back pain Ectopia lentis Hammertoe Large for gestational age Microspherophakia Cystic medial necrosis Hip dislocation Diaphragmatic eventration ST segment depression Pulmonary artery hypoplasia Rib fusion Left ventricular noncompaction cardiomyopathy Fused cervical vertebrae Cardiogenic shock Reduced systolic function Male hypogonadism Long clavicles Multiple pterygia Popliteal pterygium Camptodactyly of toe First degree atrioventricular block Abnormal left ventricle morphology Patellar aplasia Furrowed tongue Talipes calcaneovalgus Abnormality of the genital system Palpitations Arthrogryposis multiplex congenita Asthma Pulmonary hypoplasia Elevated hepatic transaminase Congenital diaphragmatic hernia Obstructive sleep apnea Distal arthrogryposis Ebstein anomaly of the tricuspid valve Neonatal respiratory distress Multiple joint contractures Vertebral fusion Dislocated radial head Hypoplastic nipples T-wave inversion Prune belly Single transverse palmar crease Mitral annular calcification Anterior clefting of vertebral bodies Dysplastic patella Medial rotation of the medial malleolus Blindness Abnormality of metabolism/homeostasis Retinopathy Pulmonary artery dilatation Proximal muscle weakness Incisional hernia Unsteady gait Increased axial length of the globe Anisometropia Overjet Spontaneous pneumothorax Inferior oblique muscle overaction Dilated cardiomyopathy Cervical C2/C3 vertebral fusion Axillary pterygium Left ventricular noncompaction Left bundle branch block Coronary artery atherosclerosis Antecubital pterygium Bilateral camptodactyly Hypoplastic heart Ventricular arrhythmia Absence of labia majora Neck pterygia Intercrural pterygium Exostosis of the external auditory canal Shock Atrial fibrillation Pulmonary arterial hypertension Hypercalcemia Dysarthria Hypercalciuria Osteopetrosis Submucous cleft hard palate Anal stenosis Fibular hypoplasia Tracheomalacia Ankylosis Pierre-Robin sequence Misalignment of teeth Thickened calvaria Echolalia Ectopic anus Thoracic dysplasia Broad ribs Large forehead Facial paralysis Natal tooth Partial agenesis of the corpus callosum Delayed closure of the anterior fontanelle Metaphyseal widening Microretrognathia Osteolysis Holoprosencephaly Mutism Pyloric stenosis Increased susceptibility to fractures Nephroblastoma Mixed hearing impairment Flat occiput Hyperostosis Delayed cranial suture closure Aphasia Dysphasia Hypoplastic left heart Visual field defect White forelock Fibular aplasia Large fontanelles Thin upper lip vermilion Vomiting Hyporeflexia Upslanted palpebral fissure Hyperactivity Respiratory failure Weight loss Photophobia Paranasal sinus hypoplasia Hypoglycemia Abnormality of the nervous system Abnormality of the pinna Pruritus Infertility Polymicrogyria Fever Straight clavicles Otosclerosis Alobar holoprosencephaly Thoracolumbar kyphosis Sclerosis of skull base Asymmetry of the thorax Flexion contracture of toe Rough bone trabeculation Broad clavicles Laryngotracheomalacia Metaphyseal striations Large iliac wings Craniofacial osteosclerosis Laryngeal web Unilateral facial palsy High iliac wings Facial hyperostosis Osteopathia striata Multicystic kidney dysplasia Aganglionic megacolon Small hand Abnormality of the thorax Hydrops fetalis Bilateral single transverse palmar creases Vasculitis Deep philtrum Bilateral ptosis Pleural effusion Cubitus valgus Cafe-au-lait spot Proximal placement of thumb Neurodevelopmental delay Abnormal eyebrow morphology Facial hypotonia Hydrocele testis Short attention span Lymphedema Hyperpigmentation of the skin Abnormality of the spleen Astigmatism Optic atrophy Splenomegaly Thrombocytopenia Postnatal growth retardation Sparse hair Abnormality of the foot Falls Fine hair Highly arched eyebrow Ascites Triangular face Lymphoma Cyanosis Epistaxis Low posterior hairline B-cell lymphoma Hypochromic microcytic anemia Omphalocele Flat face Hydronephrosis Facial palsy Ophthalmoplegia Anal atresia Cleft upper lip Thin vermilion border Delayed eruption of teeth Brachycephaly Bifid uvula Intestinal malrotation Abnormality of the skin Cerebral calcification Lumbar hyperlordosis Abnormality of the metaphysis Skeletal dysplasia Severe short stature Chylothorax Reduced factor IX activity Prominent fingertip pads Broad toe Monocytosis Pulmonary lymphangiectasia Arteritis Abnormality of the mediastinum Hypoplasia of olfactory tract Headache Reduced factor XII activity Juvenile myelomonocytic leukemia Reduced prothrombin activity Reduced factor X activity Abnormality of the subarachnoid space Hypoplasia of the corpus callosum Hydrocephalus Short palm Short foot Dysphonia Dysmetria Abnormal cardiac septum morphology Small for gestational age Corneal opacity Neurological speech impairment Malabsorption Smooth philtrum Oral cleft Blepharophimosis Postural instability Hypodontia Macroglossia Sudden cardiac death Vesicoureteral reflux Otitis media Scarring Wide mouth Microdontia Arthralgia Delayed skeletal maturation Elevated serum creatine phosphokinase Constipation Cerebellar hypoplasia Abdominal pain Cerebral cortical atrophy Coarse facial features Joint stiffness Anxiety Proteinuria Intellectual disability, moderate Developmental regression Irritability Protruding ear Autistic behavior Renal agenesis Dehydration Absent speech Ischemic stroke Abnormality of the fingernails Cutis laxa Abnormal dermatoglyphics Progressive hearing impairment Widely spaced teeth Sacral dimple Schizophrenia Nephrocalcinosis Arnold-Chiari malformation Reduced bone mineral density Adducted thumb Abnormality of pelvic girdle bone morphology Incoordination Polycystic ovaries Abnormality of dental enamel Hemivertebrae Tetralogy of Fallot Myocardial infarction Hypotelorism Hypoplasia of penis Abnormality of extrapyramidal motor function Hypsarrhythmia Renal hypoplasia Small nail Hemiparesis Pointed chin Recurrent otitis media Abnormal form of the vertebral bodies Involuntary movements Recurrent urinary tract infections Nephrolithiasis Gingival overgrowth Hoarse voice Depressivity Midface retrusion Tapered finger Hypopigmentation of hair Truncal obesity External genital hypoplasia Polyphagia Narrow nasal bridge Myeloid leukemia Impaired pain sensation Hypoventilation Skeletal muscle hypertrophy Iris hypopigmentation Central hypotonia Overweight Oligomenorrhea Acrocyanosis Hypoplasia of the fovea Adrenal insufficiency Albinism Ocular albinism Primary amenorrhea Hypopigmentation of the skin Growth hormone deficiency Febrile seizures Amenorrhea Psychosis Cutaneous photosensitivity Clumsiness Inflammation of the large intestine Bradycardia Narrow palpebral fissure Scrotal hypoplasia Hyperinsulinemia Radial deviation of finger Emotional lability Large hands Chromosome breakage Hypothermia Renal insufficiency Congenital ichthyosiform erythroderma Muscular dystrophy Ichthyosis Hepatic steatosis Scaling skin Ectropion Erythroderma Abnormality of blood and blood-forming tissues Areflexia Subcapsular cataract Congenital nonbullous ichthyosiform erythroderma Generalized ichthyosis Spasticity Hyperreflexia Tremor Hypertonia Alopecia Hepatomegaly Generalized hypopigmentation Disseminated intravascular coagulation Cor pulmonale Abdominal obesity Poor fine motor coordination Anteverted ears Frontal upsweep of hair Erysipelas Triangular mouth Acromicria Temperature instability Central adrenal insufficiency Hypoplastic labia minora Psychotic episodes Narrow palm Almond-shaped palpebral fissure Poor gross motor coordination Abnormal B-type natriuretic peptide level


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