Fever, and Pectus carinatum

Diseases related with Fever and Pectus carinatum

In the following list you will find some of the most common rare diseases related to Fever and Pectus carinatum that can help you solving undiagnosed cases.

Top matches:

EXTRAORAL HALITOSIS DUE TO METHANETHIOL OXIDASE DEFICIENCY; EHMTO Is also known as extraoral halitosis with dimethylsulfoxiduria|methanethiol oxidase deficiency|mto deficiency

Related symptoms:

  • Global developmental delay
  • Scoliosis
  • Ptosis
  • Fever
  • Skeletal muscle atrophy


SOURCES: OMIM MENDELIAN

More info about EXTRAORAL HALITOSIS DUE TO METHANETHIOL OXIDASE DEFICIENCY; EHMTO

Malignant hyperthermia susceptibility (MHS), a skeletal muscle disorder most often inherited as an autosomal dominant trait, is one of the main causes of death due to anesthesia. In susceptible people, a malignant hyperthermia episode is triggered by exposure to commonly used volatile anesthetic agents such as halothane or depolarizing muscle relaxants such as succinyl choline. A fulminant MH crisis is characterized by any combination of hyperthermia, skeletal muscle rigidity, tachycardia or arrhythmia, respiratory and metabolic acidosis, and rhabdomyolysis. Except for this susceptibility to triggering agents, MHS patients are not clinically distinguishable from the general population (summary by Monnier et al., 1997). Genetic Heterogeneity of Susceptibility to Malignant HyperthermiaOther MHS loci include MHS2 (OMIM ) on chromosome 17q; MHS3 (OMIM ) on chromosome 7q; MHS4 (OMIM ) on chromosome 3q; MHS5 (OMIM ), caused by mutation in the CACNA1S gene (OMIM ) on chromosome 1q32; and MHS6 (OMIM ) on chromosome 5p.

MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 1; MHS1 Is also known as mhs|hyperthermia of anesthesia|mh|hyperpyrexia, malignant

Related symptoms:

  • Intellectual disability
  • Seizures
  • Short stature
  • Generalized hypotonia
  • Scoliosis


SOURCES: OMIM MENDELIAN

More info about MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 1; MHS1

SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1 Is also known as sja syndrome|schwartz-jampel-aberfeld syndrome|sjs|myotonic myopathy, dwarfism, chondrodystrophy, and ocular and facial abnormalities|schwartz-jampel syndrome|chondrodystrophic myotonia

Related symptoms:

  • Intellectual disability
  • Short stature
  • Generalized hypotonia
  • Microcephaly
  • Growth delay


SOURCES: OMIM MENDELIAN

More info about SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1

Other less relevant matches:

Larsen-like syndrome, B3GAT3 type is a rare, genetic, primary bone dysplasia characterized by laxity, dislocations and contractures of the joints, short stature, foot deformities (e.g. clubfeet), broad tips of fingers and toes, short neck, dysmorphic facial features (hypertelorism, downslanting palpebral fissures, upturned nose with anteverted nares, high arched palate) and various cardiac malformations. Severe disease is associated with multiple fractures, osteopenia, arachnodactyly and blue sclerae. A broad spectrum of additional features, including scoliosis, radio-ulnar synostosis, mild developmental delay, and various eye disorders (glaucoma, amblyopia, hyperopia, astigmatism, ptosis), are also reported.

LARSEN-LIKE SYNDROME, B3GAT3 TYPE Is also known as multiple joint dislocations-short stature-craniofacial dysmorphism-congenital heart defects syndrome|larsen syndrome, autosomal recessive, formerly

Related symptoms:

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


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about LARSEN-LIKE SYNDROME, B3GAT3 TYPE

Mowat-Wilson syndrome is an autosomal dominant complex developmental disorder; individuals with functional null mutations present with mental retardation, delayed motor development, epilepsy, and a wide spectrum of clinically heterogeneous features suggestive of neurocristopathies at the cephalic, cardiac, and vagal levels. Mowat-Wilson syndrome has many clinical features in common with Goldberg-Shprintzen syndrome (OMIM ) but the 2 disorders are genetically distinct (Mowat et al., 2003). Goldberg-Shprintzen syndrome is caused by mutation in the KIAA1279 gene (OMIM ) located on 10q.

MOWAT-WILSON SYNDROME; MOWS Is also known as microcephaly, mental retardation, and distinct facial features, with or without hirschsprung disease|hirschsprung disease-mental retardation syndrome

Related symptoms:

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


SOURCES: ORPHANET OMIM MENDELIAN

More info about MOWAT-WILSON SYNDROME; MOWS

Noonan syndrome (NS) is an autosomal dominant disorder characterized by short stature, facial dysmorphism, and a wide spectrum of congenital heart defects. The distinctive facial features consist of a broad forehead, hypertelorism, downslanting palpebral fissures, a high-arched palate, and low-set, posteriorly rotated ears. Cardiac involvement is present in up to 90% of patients. Pulmonic stenosis and hypertrophic cardiomyopathy are the most common forms of cardiac disease, but a variety of other lesions are also observed. Additional relatively frequent features include multiple skeletal defects (chest and spine deformities), webbed neck, mental retardation, cryptorchidism, and bleeding diathesis (summary by Tartaglia et al., 2002). Genetic Heterogeneity of Noonan SyndromeSee also NS3 (OMIM ), caused by mutation in the KRAS gene (OMIM ); NS4 (OMIM ), caused by mutation in the SOS1 gene (OMIM ); NS5 (OMIM ), caused by mutation in the RAF1 gene (OMIM ); NS6 (OMIM ), caused by mutation in the NRAS gene (OMIM ); NS7 (OMIM ), caused by mutation in the BRAF gene (OMIM ); NS8 (OMIM ), caused by mutation in the RIT1 gene (OMIM ); NS9 (OMIM ), caused by mutation in the SOS2 gene (OMIM ); and NS10 (OMIM ), caused by mutation in the LZTR1 gene (OMIM ).See also NS2 (OMIM ) for a possible autosomal recessive form of NS; Noonan syndrome-like disorder with loose anagen hair-1 (NSLH1 ), caused by mutation in the SHOC2 gene (OMIM ); Noonan syndrome-like disorder with loose anagen hair-2 (NSLH2 ), caused by mutation in the PPP1CB gene (OMIM ); and Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia (NSLL ), caused by mutation in the CBL gene (OMIM ).Mutations in the neurofibromin gene (NF1 ), which is the site of mutations causing classic neurofibromatosis type I (NF1 ), have been found in neurofibromatosis-Noonan syndrome (NFNS ).

NOONAN SYNDROME 1; NS1 Is also known as female pseudo-turner syndrome|male turner syndrome|noonan syndrome|turner phenotype with normal karyotype

Related symptoms:

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


SOURCES: OMIM MENDELIAN

More info about NOONAN SYNDROME 1; NS1

Medium match H SYNDROME

H syndrome is a systemic inherited histiocytosis, with characteristic cutaneous findings accompanying systemic manifestations. H syndrome refers to the major clinical findings of hyperpigmentation, hypertrichosis, hepatosplenomegaly, heart anomalies, hearing loss, hypogonadism, low height, and occasionally, hyperglycemia/diabetes mellitus. Due to overlapping clinical features, H syndrome is now considered to include pigmented hypertrichosis with insulin dependent diabetes mellitus syndrome (PHID), Faisalabad histiocytosis (FHC) and familial sinus histiocytosis with massive lymphadenopathy (FSHML).

H SYNDROME Is also known as sinus histiocytosis and massive lymphadenopathy|hjcd|shml|hyperpigmentation, cutaneous, with hypertrichosis, hepatosplenomegaly, heart anomalies, and hypogonadism with or without hearing loss|h syndrome|faisalabad histiocytosis|pigmented hypertrichosis wi

Related symptoms:

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


SOURCES: MESH ORPHANET OMIM MENDELIAN

More info about H SYNDROME

Ulnar-mammary syndrome (UMS) is a rare developmental disorder characterized by ulnar defects, mammary and apocrine gland hypoplasia and genital anomalies. Delayed puberty dental anomalies, short stature and obesity have also been described.

ULNAR-MAMMARY SYNDROME Is also known as schinzel syndrome|ums|pallister ulnar-mammary syndrome

Related symptoms:

  • Short stature
  • Growth delay
  • Hypertelorism
  • Cryptorchidism
  • Ptosis


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about ULNAR-MAMMARY SYNDROME

Occipital horn syndrome (OHS) is a mild form of Menkes disease (MD, see this term), a syndrome characterized by progressive neurodegeneration and connective tissue disorders due to a copper transport defect.

OCCIPITAL HORN SYNDROME Is also known as eds ix, formerly|eds ix|ehlers-danlos syndrome type ix|ehlers-danlos syndrome type 9|x-linked cutis laxa|ehlers-danlos syndrome, occipital horn type, formerly|eds9, formerly|cutis laxa, x-linked, formerly

Related symptoms:

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


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about OCCIPITAL HORN SYNDROME

Schwartz-Jampel syndrome (SJS) is characterised by myotonia and osteoarticular abnormalities.

SCHWARTZ-JAMPEL SYNDROME Is also known as myotonic chondrodystrophy|schwartz-jampel-aberfeld syndrome|burton skeletal dysplasia|sjs|myotonic myopathy, dwarfism, chondrodystrophy, ocular and facial anomalies|dysostosis enchondralis metaepiphysaria, catel-hempel type|burton syndrome|aberfeld syndro

Related symptoms:

  • Intellectual disability
  • Short stature
  • Microcephaly
  • Scoliosis
  • Hypertelorism


SOURCES: ORPHANET MENDELIAN

More info about SCHWARTZ-JAMPEL SYNDROME

Top 5 symptoms//phenotypes associated to Fever and Pectus carinatum

Symptoms // Phenotype % cases
Ptosis Very Common - Between 80% and 100% cases
Short stature Common - Between 50% and 80% cases
Hypertelorism Common - Between 50% and 80% cases
Intellectual disability Common - Between 50% and 80% cases
Abnormal facial shape Common - Between 50% and 80% cases

Other less frequent symptoms

Patients with Fever and Pectus carinatum. may also develop some of the following symptoms:

Common Symptoms - More than 50% cases

Generalized hypotonia

Uncommon Symptoms - Between 30% and 50% cases

Global developmental delay

Common Symptoms - More than 50% cases

Growth delay

Uncommon Symptoms - Between 30% and 50% cases

Ventricular septal defect Scoliosis Pes planus Downslanted palpebral fissures High palate Flexion contracture Inguinal hernia Hernia Pectus excavatum Seizures Microcephaly Short neck Talipes equinovarus Delayed skeletal maturation Micrognathia Osteoporosis Proptosis Flat face Kyphoscoliosis Malignant hyperthermia Dilatation Abnormal heart morphology Abnormal cardiac septum morphology Epicanthus Skeletal muscle atrophy Low-set ears Cryptorchidism Strabismus Frontal bossing Coxa vara Patent ductus arteriosus Cataract Pain Wide nasal bridge Hearing impairment Posteriorly rotated ears Cleft palate Myopia Narrow mouth Osteopenia Umbilical hernia Pulmonic stenosis Apnea Camptodactyly Atrial septal defect Platyspondyly Genu valgum Blue sclerae Recurrent fractures Full cheeks Decreased testicular size Elbow flexion contracture Poor suck Coxa valga Muscular hypotonia Hyperhidrosis Brachydactyly Lymphedema Low-set, posteriorly rotated ears Abnormal eyebrow morphology Kyphosis Myotonia Muscle weakness Myopathy Webbed neck Intellectual disability, mild Arrhythmia Midface retrusion

Rare Symptoms - Less than 30% cases

Left ventricular hypertrophy Amblyopia Cutis laxa Bicuspid aortic valve Hyperextensible skin Patent foramen ovale Wormian bones Amenorrhea Hip dysplasia Nystagmus Wide intermamillary distance Primary amenorrhea Bifid scrotum Low posterior hairline Congestive heart failure Delayed puberty Motor delay Micropenis Osteolysis Leukocytosis Anteverted nares Hydrocephalus Cerebral cortical atrophy Cardiomegaly Joint laxity Azoospermia Hip dislocation Narrow chest Abnormality of the foot Plagiocephaly Failure to thrive Mitral valve prolapse Esotropia Hypotrichosis Dental malocclusion Camptodactyly of finger Short clavicles Mandibular prognathia High forehead Hydronephrosis Anxiety Abnormality of the kidney Sprengel anomaly Neurological speech impairment Broad eyebrow Cleft upper lip Everted lower lip vermilion Hallux valgus Abdominal distention Coarctation of aorta Abnormality of the genital system Abnormality of the wrist Short humerus Constipation High, narrow palate Clinodactyly Ventriculomegaly Bruising susceptibility Pyloric stenosis Gastroesophageal reflux Polyhydramnios Hypogonadism Intellectual disability, severe Splenomegaly Subglottic stenosis Edema Vomiting Convex nasal ridge Diarrhea Abnormality of cardiovascular system morphology Sensorineural hearing impairment Long philtrum Laryngomalacia Postnatal growth retardation Growth hormone deficiency Depressed nasal bridge Severe short stature Sleep apnea Generalized hirsutism EMG abnormality Hypertonia Abnormality of the coagulation cascade Malar flattening Bowing of the long bones Microcornea Talipes Elevated serum creatine phosphokinase Blepharophimosis Skeletal dysplasia Hyporeflexia Skeletal muscle hypertrophy Rigidity Respiratory distress Abnormality of the skeletal system Dysphagia Myalgia Hyperlordosis Arthrogryposis multiplex congenita Tachycardia Joint hypermobility Low hanging columella Abnormal bleeding Lumbar hyperlordosis Acute kidney injury Overfolded helix Renal insufficiency High pitched voice Blepharospasm Long eyelashes in irregular rows Pneumonia Generalized muscle hypertrophy Shoulder flexion contracture Pursed lips Bilateral ptosis Weak voice Wrist flexion contracture Flexion contracture of toe Hip contracture Episodic fever Abnormality of the pharynx Hypoplasia of penis Abnormality of the ureter Overgrowth Postaxial hand polydactyly Trismus Aplasia/Hypoplasia affecting the eye Increased antibody level in blood Round face Elevated erythrocyte sedimentation rate Hypodontia Renal hypoplasia Postaxial polydactyly Distichiasis Wide nose Bilateral sensorineural hearing impairment Short distal phalanx of finger Abnormally ossified vertebrae Protrusio acetabuli Anal atresia Epidermal acanthosis Polydactyly Interphalangeal joint contracture of finger Split hand Obesity Spinal rigidity Abnormality of the clavicle Ectopia lentis Elbow dislocation Inverted nipples Shawl scrotum Mask-like facies Absent radius Anal stenosis Oligodactyly Hypoplastic nipples Hyperthyroidism Abnormality of the fingernails Decreased fertility Stridor External genital hypoplasia Hypoplasia of the ulna Hypoplastic toenails Increased number of teeth Hyperglycemia Hand polydactyly Abnormality of immune system physiology Hypoplasia of the radius Abnormality of the metacarpal bones Upslanted palpebral fissure Epistaxis Severe sensorineural hearing impairment Reticulocytopenia Facial telangiectasia Testicular torsion Myelofibrosis Generalized lymphadenopathy Corneal arcus Hyperplasia of the maxilla Broad finger Pancreatic hypoplasia Abnormality of cardiovascular system physiology Chronic rhinitis Histiocytosis Episcleritis Skin nodule Nasal obstruction Recurrent pharyngitis Decreased serum testosterone level Communicating hydrocephalus Varicose veins Aspiration pneumonia Enlarged kidney Exocrine pancreatic insufficiency Polycythemia Lipodystrophy Panniculitis Snoring Hypertriglyceridemia Lipoatrophy Hypertrichosis Abnormality of the dentition Metatarsus valgus Microcytic anemia Psoriasiform dermatitis Seborrheic keratosis Prenatal movement abnormality Odontogenic neoplasm Bronchiectasis Telangiectasia Gingival overgrowth Stiff skin Scleroderma Hyperpigmentation of the skin Gynecomastia Aspiration Retroperitoneal fibrosis Hypergonadotropic hypogonadism Upper eyelid edema Type I diabetes mellitus Elevated aldolase level Bilateral camptodactyly Cervical lymphadenopathy Abnormality of finger Breast hypoplasia Hypoplastic scapulae Orthostatic hypotension Premature skin wrinkling Hypothermia Esophagitis Down-sloping shoulders Atypical scarring of skin Abnormality of the skull Hiatus hernia Carpal synostosis Soft skin Exostoses Dislocated radial head Polyneuropathy Limited elbow extension Visual impairment Delayed cranial suture closure Rickets Redundant skin Coarse hair Gait disturbance Narrow face Dental crowding Chronic diarrhea Large fontanelles Abnormality of the face Recurrent urinary tract infections Cholestasis Generalized joint laxity Humerus varus Cerebral calcification Abnormality of esophagus physiology Aplasia/hypoplasia of the humerus Rudimentary to absent tibiae Pelvic bone exostoses Bladder carcinoma Abnormality of the pubic bone Large iliac wings Broad clavicles Limited knee extension Persistent open anterior fontanelle Long neck Synostosis of joints Ureteral obstruction Aortic rupture Broad ribs Absent tibia Abnormality of the sense of smell Keloids Gastroparesis Aplastic clavicle Thick hair Femoral hernia Carotid artery tortuosity Venous insufficiency Bladder diverticulum Abnormality of fibula morphology Avascular necrosis of the capital femoral epiphysis Prominent superficial veins Hepatitis Specific learning disability Cachexia Abnormality of the humerus Body odor Aplasia of the ulna Ectopic posterior pituitary Absent hand Abnormality of the radius Abnormality of temperature regulation Laryngeal stenosis Aplasia/Hypoplasia of the ulna Increased bone mineral density Gastroschisis Breast aplasia Anterior pituitary hypoplasia Wide nasal base Abnormal external genitalia Capitate-hamate fusion Perimembranous ventricular septal defect Gonadotropin deficiency Broad face Abnormality of the uterus Wolff-Parkinson-White syndrome Sparse lateral eyebrow Sparse axillary hair Low anterior hairline Dysphonia Supraventricular tachycardia Ectopic anus Abnormality of the urinary system Abnormality of epiphysis morphology Absent axillary hair Respiratory insufficiency Axillary apocrine gland hypoplasia Short palm Long face Joint hyperflexibility Dolichocephaly Scarring Abnormality of the pinna Jaundice Feeding difficulties in infancy Unilateral oligodactyly Irritability Joint stiffness Attention deficit hyperactivity disorder Deformed radius Nephrolithiasis Prominent nasal bridge Micromelia Long uvula Abnormality of the ribs Pulmonary arterial hypertension Short 5th toe Abnormality of the metaphysis Short 4th toe Imperforate hymen Decreased body weight Aplasia of the pectoralis major muscle Laryngeal web Hernia of the abdominal wall Osteomalacia Neoplasm Ichthyosis Congenital glaucoma Abnormality of the abdominal wall Endocardial fibroelastosis Deep palmar crease Small face Generalized osteoporosis 11 pairs of ribs Overlapping fingers Abnormally large globe Upper limb undergrowth Aortic root aneurysm Narrow nasal bridge Restrictive ventilatory defect Thoracic hypoplasia Knee dislocation Bilateral talipes equinovarus Metatarsus adductus Spondyloepiphyseal dysplasia Radioulnar synostosis Sandal gap Accelerated skeletal maturation Microretrognathia Joint dislocation Meningitis Rhizomelia Abnormal lung morphology Mitral regurgitation Lumbar scoliosis Talipes equinovalgus Microdontia Microphthalmia Falls Abnormality of the cerebral white matter Finger syndactyly Short philtrum Coloboma Telecanthus Deeply set eye Macrotia Agenesis of corpus callosum Depressivity Hypospadias Absent speech Syndactyly Multiple joint dislocation Short nose Behavioral abnormality Hypoplasia of the corpus callosum Bilateral elbow dislocations Metacarpophalangeal joint hyperextensibility Broad distal phalanges of all fingers Spatulate thumbs Prominent antitragus Enlarged metaphyses Accessory carpal bones Hypertropia Shoulder dislocation Congenital diaphragmatic hernia Short metacarpal Tapered finger Shock Hyperphosphatemia Thoracic kyphosis Myoglobinuria Scaphocephaly Rhabdomyolysis Abnormality of the sternum Hyperkalemia Myopathic facies Ventricular fibrillation Deep philtrum Ventricular arrhythmia Tachypnea Decreased fetal movement Severe lactic acidosis Hypotension Muscle cramps Metabolic acidosis Lactic acidosis Limb muscle weakness Muscular dystrophy Stroke Proximal muscle weakness Acidosis Pes cavus Halitosis Muscle fibrillation Breech presentation Respiratory arrest Thick eyebrow Spinal deformities Arachnodactyly Hypermetropia Microtia Glaucoma Brachycephaly Prominent forehead Anterior bowing of long bones Abnormality of femoral epiphysis Smooth tongue Percussion myotonia Talipes valgus Temperature instability Hypoplasia of the musculature Diaphragmatic eventration Coronal cleft vertebrae Constrictive median neuropathy Metaphyseal widening Narrow palpebral fissure Congenital hip dislocation Abnormal autonomic nervous system physiology Joint contracture of the hand Hypertension Mixed respiratory and metabolic acidosis Sinus tachycardia Long upper lip Congenital ptosis Iris coloboma Delayed eruption of teeth Lymphadenopathy Male infertility Schwannoma Synovitis Shield chest Restrictive cardiomyopathy Atrial flutter Nonimmune hydrops fetalis Drusen Arnold-Chiari type I malformation Gonadal dysgenesis Abnormality of blood and blood-forming tissues Neuroblastoma Abnormality of the vertebral column Cystic hygroma Asymmetry of the thorax Neurofibromas Abnormality of color vision Radial deviation of finger Cubitus valgus Myelodysplasia Failure to thrive in infancy Elevated alkaline phosphatase Pterygium Arnold-Chiari malformation Clumsiness Ventricular hypertrophy Triangular face Multiple lentigines Optic disc hypoplasia Leukemia Postductal coarctation of the aorta Malabsorption Retinopathy Conductive hearing impairment Hepatosplenomegaly Dyspnea Hypothyroidism Hyperkeratosis Diabetes mellitus Alopecia Hepatomegaly Hyperreflexia Anemia Preductal coarctation of the aorta Lymphangioma Nasogastric tube feeding Reduced factor XIII activity Gonadal neoplasm Pectus excavatum of inferior sternum Loose anagen hair Juvenile myelomonocytic leukemia Panuveitis Neurofibrosarcoma Reduced factor XII activity Superior pectus carinatum Amegakaryocytic thrombocytopenia Hypoplastic aortic arch Facial asymmetry Broad forehead Brain atrophy Pointed chin Supernumerary nipple Ectopic kidney Rocker bottom foot Cupped ear Aplasia/Hypoplasia of the cerebellum Sparse eyebrow Abnormality of the genitourinary system Drooling Aplasia/Hypoplasia of the corpus callosum Widely spaced teeth Cutaneous syndactyly Absence seizures Postnatal microcephaly Drowsiness Aganglionic megacolon Recurrent otitis media Open mouth Sparse scalp hair Fine hair Sloping forehead Dehydration Tetralogy of Fallot Febrile seizures Focal-onset seizure Otitis media Vesicoureteral reflux Submucous cleft hard palate External ear malformation Sparse hair Abnormal eye morphology Hypertrophic cardiomyopathy Abdominal pain Rod-cone dystrophy Thrombocytopenia Headache Cardiomyopathy Feeding difficulties Cognitive impairment Aplasia/Hypoplasia of the cerebral white matter Pulmonary artery sling Large basal ganglia Abnormal morphology of the hippocampus Uplifted earlobe Pulmonary artery stenosis Atypical absence seizures Happy demeanor Deep plantar creases Prominent nasal tip Esodeviation Broad columella Broad hallux phalanx Large earlobe Bruxism Abnormality of the gastrointestinal tract Tracheal stenosis Misalignment of teeth Chronic constipation Abnormally straight spine


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