Fever, and Dental crowding

Diseases related with Fever and Dental crowding

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

Top matches:

The newly described 2q23.1 microdeletion syndrome includes severe intellectual deficit with pronounced speech delay, behavioral abnormalities including hyperactivity and inappropriate laughter, short stature and seizures.

2Q23.1 MICRODELETION SYNDROME Is also known as pseudo-angelman syndrome|del(2)(q23.1)|monosomy 2q23.1

Related symptoms:

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


SOURCES: ORPHANET OMIM MENDELIAN

More info about 2Q23.1 MICRODELETION SYNDROME

Smith-Lemli-Opitz syndrome (SLOS) is characterized by multiple congenital anomalies, intellectual deficit, and behavioral problems.

SMITH-LEMLI-OPITZ SYNDROME Is also known as rutledge lethal multiple congenital anomaly syndrome|slos|lethal acrodysgenital syndrome|rsh syndrome|slo syndrome|7-dehydrocholesterol reductase deficiency|polydactyly, sex reversal, renal hypoplasia, and unilobar lung

Related symptoms:

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


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about SMITH-LEMLI-OPITZ SYNDROME

Phelan-McDermid syndrome is a developmental disorder with variable features. Common features include neonatal hypotonia, global developmental delay, normal to accelerated growth, absent to severely delayed speech, autistic behavior (see {209850}), and minor dysmorphic features (Precht et al., 1998; Prasad et al., 2000; Durand et al., 2007).

PHELAN-MCDERMID SYNDROME; PHMDS Is also known as chromosome 22q13.3 deletion syndrome|telomeric 22q13 monosomy syndrome

Related symptoms:

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


SOURCES: ORPHANET MESH OMIM MENDELIAN

More info about PHELAN-MCDERMID SYNDROME; PHMDS

Other less relevant matches:

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

Hirschsprung disease (HSCR) is a congenital intestinal motility disorder that is characterized by signs of intestinal obstruction due to the presence of an aganglionic segment of variable extent in the terminal part of the colon.

HIRSCHSPRUNG DISEASE Is also known as hscr|aganglionic megacolon|congenital intestinal aganglionosis|hirschsprung disease|megacolon, aganglionic|mgc

Related symptoms:

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


SOURCES: ORPHANET OMIM MENDELIAN

More info about HIRSCHSPRUNG DISEASE

Angelman syndrome is a neurodevelopmental disorder characterized by mental retardation, movement or balance disorder, typical abnormal behaviors, and severe limitations in speech and language. Most cases are caused by absence of a maternal contribution to the imprinted region on chromosome 15q11-q13. Prader-Willi syndrome (PWS ) is a clinically distinct disorder resulting from paternal deletion of the same 15q11-q13 region. In addition, the chromosome 15q11-q13 duplication syndrome (OMIM ) shows overlapping clinical features.Clayton-Smith and Pembrey (1992) provided a review of Angelman syndrome. Cassidy and Schwartz (1998) reviewed the molecular and clinical aspects of both Prader-Willi syndrome and Angelman syndrome. Horsthemke and Wagstaff (2008) provided a detailed review of the mechanisms of imprinting of the Prader-Willi/Angelman syndrome region.Van Buggenhout and Fryns (2009) provided a review of Angelman syndrome and discussed genetic counseling of the disorder, which can show a recurrence risk of up to 50%, depending on the underlying genetic mechanism.

ANGELMAN SYNDROME; AS Is also known as happy puppet syndrome, formerly

Related symptoms:

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


SOURCES: ORPHANET OMIM MENDELIAN

More info about ANGELMAN SYNDROME; AS

Freeman-Sheldon syndrome (FSS), or DA2A, is phenotypically similar to DA1. In addition to contractures of the hands and feet, FSS is characterized by oropharyngeal abnormalities, scoliosis, and a distinctive face that includes a very small oral orifice (often only a few millimeters in diameter at birth), puckered lips, and an H-shaped dimple of the chin; hence, FSS has been called 'whistling face syndrome.' The limb phenotypes of DA1 and FSS may be so similar that they can only be distinguished by the differences in facial morphology (summary by Bamshad et al., 2009).For a general phenotypic description and a discussion of genetic heterogeneity of distal arthrogryposis, see DA1 (OMIM ).

ARTHROGRYPOSIS, DISTAL, TYPE 2A; DA2A Is also known as craniocarpotarsal dysplasia|fss|craniocarpotarsal dystrophy|whistling face-windmill vane hand syndrome|freeman-sheldon syndrome

Related symptoms:

  • Intellectual disability
  • Seizures
  • Short stature
  • Generalized hypotonia
  • Hearing impairment


SOURCES: OMIM MENDELIAN

More info about ARTHROGRYPOSIS, DISTAL, TYPE 2A; DA2A

Fibrodysplasia ossificans progressiva (FOP) is a severely disabling heritable disorder of connective tissue characterized by congenital malformations of the great toes and progressive heterotopic ossification that forms qualitatively normal bone in characteristic extraskeletal sites.

FIBRODYSPLASIA OSSIFICANS PROGRESSIVA Is also known as stone man syndrome|fop|myositis ossificans progressiva

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Hearing impairment
  • Scoliosis


SOURCES: OMIM ORPHANET MENDELIAN

More info about FIBRODYSPLASIA OSSIFICANS PROGRESSIVA

Low match OHDO SYNDROME

OHDO SYNDROME Is also known as ohdo blepharophimosis syndrome|mental retardation, congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth

Related symptoms:

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


SOURCES: OMIM MENDELIAN

More info about OHDO SYNDROME

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

Top 5 symptoms//phenotypes associated to Fever and Dental crowding

Symptoms // Phenotype % cases
Intellectual disability Very Common - Between 80% and 100% cases
Global developmental delay Very Common - Between 80% and 100% cases
Seizures Very Common - Between 80% and 100% cases
Generalized hypotonia Common - Between 50% and 80% cases
Microcephaly Common - Between 50% and 80% cases

Other less frequent symptoms

Patients with Fever and Dental crowding. may also develop some of the following symptoms:

Common Symptoms - More than 50% cases

Hearing impairment

Uncommon Symptoms - Between 30% and 50% cases

Ptosis

Common Symptoms - More than 50% cases

Short stature

Uncommon Symptoms - Between 30% and 50% cases

Muscular hypotonia

Common Symptoms - More than 50% cases

Feeding difficulties

Uncommon Symptoms - Between 30% and 50% cases

Scoliosis

Common Symptoms - More than 50% cases

Failure to thrive

Uncommon Symptoms - Between 30% and 50% cases

Vomiting

Common Symptoms - More than 50% cases

Constipation

Uncommon Symptoms - Between 30% and 50% cases

Strabismus

Common Symptoms - More than 50% cases

High palate

Uncommon Symptoms - Between 30% and 50% cases

Short nose Epicanthus Long philtrum Wide nasal bridge Diarrhea Widely spaced teeth Gastroesophageal reflux Micrognathia Cryptorchidism Behavioral abnormality Intellectual disability, severe Feeding difficulties in infancy Patent ductus arteriosus Flexion contracture Motor delay Kyphosis Low-set ears Ventricular septal defect Atrial septal defect Pain Autistic behavior Hydronephrosis Deeply set eye Autism Abnormal facial shape Sensorineural hearing impairment Clinodactyly of the 5th finger Sleep disturbance Hypertelorism Hyperactivity Downslanted palpebral fissures Abnormality of cardiovascular system morphology Ventriculomegaly Nystagmus Cleft palate Dental malocclusion Optic atrophy Self-injurious behavior Anxiety Absent speech Talipes equinovarus Focal-onset seizure Bulbous nose Intellectual disability, mild Postnatal growth retardation Aggressive behavior EEG abnormality Aganglionic megacolon Abnormality of the genital system Retrognathia Hypermetropia Adducted thumb Sloping forehead Inguinal hernia Intellectual disability, profound Thick eyebrow Poor suck Malar flattening Hip dislocation Glaucoma Growth delay Posteriorly rotated ears Ataxia Mandibular prognathia Wide mouth

Rare Symptoms - Less than 30% cases

Coarctation of aorta Recurrent otitis media Submucous cleft hard palate Renal cyst Aplasia/Hypoplasia of the cerebellum Abnormality of the dentition Overbite Atrioventricular canal defect Hallux valgus Bifid scrotum Pyloric stenosis Tracheal stenosis Breech presentation Rocker bottom foot Macrocephaly Scrotal hypoplasia Sleep-wake cycle disturbance Aplasia/Hypoplasia of the corpus callosum Multicystic kidney dysplasia Short thumb 2-3 toe syndactyly Blepharophimosis Happy demeanor Telecanthus Joint hyperflexibility Cerebral cortical atrophy Cerebellar atrophy Abnormality of the skeletal system Dilatation Pectus excavatum High forehead Joint laxity Pectus carinatum Long nose Tongue thrusting Specific learning disability Flat occiput Abnormality of the face Abdominal distention Myopathy Neoplasm Exostoses Synostosis of joints Neurological speech impairment Falls Obesity Vesicoureteral reflux Narrow mouth Agenesis of corpus callosum Macrotia Umbilical hernia Abnormality of the pinna Dolichocephaly Nausea and vomiting High, narrow palate Hepatitis Bruxism Broad-based gait Iris coloboma Long eyelashes Chronic diarrhea Pointed chin Drowsiness Drooling Aspiration Postnatal microcephaly Hypopigmentation of the skin Bladder diverticulum Polyphagia Severe short stature Clinodactyly Low anterior hairline Febrile seizures Polyhydramnios Brachycephaly Gait ataxia Hypertonia Protruding ear Microtia Syndactyly Open mouth Hypoplasia of penis Frontal bossing Hip dysplasia Facial asymmetry Microphthalmia Abnormal heart morphology Astigmatism Short palm Short attention span Hypospadias Everted lower lip vermilion Recurrent infections Prominent nose Encephalopathy Esotropia Intellectual disability, moderate Short chin Short neck Myopia Hypoplasia of the corpus callosum Brachydactyly Finger syndactyly Depressed nasal bridge Delayed speech and language development Spasticity Absence seizures Anteverted nares Abnormality of the kidney Finger clinodactyly Cupped ear Paroxysmal bursts of laughter Anisometropia Clumsiness Hypoplasia of the maxilla Status epilepticus Abnormal cerebellum morphology Limb tremor Large foramen magnum Misalignment of teeth Inappropriate laughter Macroglossia Overgrowth Broad eyebrow Generalized-onset seizure Intellectual disability, progressive Abnormality of the gastrointestinal tract Broad columella Fair hair Blue irides Progressive gait ataxia Esodeviation Epileptic spasms Profound global developmental delay Overweight Moderate global developmental delay Atonic seizures Exotropia Broad hallux phalanx Keratoconus Albinism Incoordination Hyperkinesis Prominent nasal tip Cerebral palsy Large earlobe Protruding tongue Abnormality of the cerebral white matter Infertility Bladder carcinoma Weight loss Abdominal pain Hypogonadism Humerus varus Carotid artery tortuosity Aortic rupture Abnormality of esophagus physiology Ureteral obstruction Persistent open anterior fontanelle Limited knee extension Pulmonary artery sling Pelvic bone exostoses Lethargy Rudimentary to absent tibiae Aplasia/hypoplasia of the humerus Capitate-hamate fusion Abnormality of the pubic bone Large iliac wings Broad clavicles Long neck Absent tibia Abnormality of the sense of smell Keloids Gastroparesis Aplastic clavicle Prominent nasal bridge Sepsis Abnormality of movement Anteverted ears Subglottic stenosis Deep plantar creases Hyperreflexia Atypical absence seizures Abnormality of enteric ganglion morphology Uplifted earlobe Intestinal perforation Functional abnormality of the gastrointestinal tract Neoplasm of the thyroid gland Total colonic aganglionosis Generalized muscle hypertrophy Abnormal eye morphology Increased body weight Central hypoventilation Enterocolitis Intestinal polyposis Neoplasm of the endocrine system Heterochromia iridis Hypoventilation Abnormal morphology of the hippocampus Malnutrition Large basal ganglia Intestinal obstruction Failure to thrive in infancy Abnormal autonomic nervous system physiology Total intestinal aganglionosis External ear malformation Muscle weakness Sparse scalp hair Abnormality of the foot Proteinuria Hypothyroidism Recurrent respiratory infections Aplasia/Hypoplasia of the phalanges of the hallux Dehydration Abnormality of the first metatarsal bone Progressive cervical vertebral spine fusion Ectopic ossification in tendon tissue Ectopic ossification in ligament tissue Ectopic ossification in muscle tissue Fine hair Small cervical vertebral bodies Smooth philtrum Ectopic ossification Fibrosarcoma Osteochondroma Thick hair Low-grade fever Cutaneous syndactyly Stiff neck Broad femoral neck Short 1st metacarpal Short hallux Abnormality of the genitourinary system Myositis Tetralogy of Fallot Otitis media Ankylosis Hypoplasia of teeth Cleft upper lip Short philtrum Camptodactyly of finger Abnormal cardiac septum morphology Coloboma Depressivity Abnormality of the cheek Neoplasm of the tongue Thyroid agenesis Ectopic thyroid Thyroid hypoplasia Abnormal nasolacrimal system morphology Abnormality of the antihelix Thin vermilion border Stenosis of the external auditory canal Tapered finger Prominent occiput Delayed eruption of teeth Bilateral single transverse palmar creases Sparse and thin eyebrow Short palpebral fissure Interphalangeal joint contracture of finger Hypsarrhythmia Brain atrophy Bifid uvula Triangular face Broad neck Alopecia of scalp Chronic constipation Flat face Mask-like facies Hypoplasia of the brainstem Congenital contracture Rheumatoid arthritis Pterygium Nasal speech Spina bifida occulta Knee flexion contracture Joint contracture of the hand Sparse eyebrow Abnormality of the skin Underdeveloped nasal alae Talipes Atrophy/Degeneration affecting the brainstem Arthrogryposis multiplex congenita Small for gestational age Ectopic kidney Camptodactyly Supernumerary nipple Arthritis Kyphoscoliosis Pulmonic stenosis Pulmonary artery stenosis Abnormal eyebrow morphology Low hanging columella Prominent forehead Hip contracture Distal arthrogryposis Basal ganglia calcification Difficulty walking Hamartoma Spinal rigidity Metaphyseal widening Back pain Sarcoma Abnormal vertebral morphology Subcutaneous nodule Myocardial infarction Limitation of joint mobility Hypotrichosis Respiratory tract infection Conductive hearing impairment Respiratory failure Malignant hyperthermia Pneumonia Alopecia Congestive heart failure Respiratory insufficiency Anemia Chin with H-shaped crease Whistling appearance Shoulder flexion contracture Ulnar deviation of the hand or of fingers of the hand Abnormal auditory evoked potentials Flexion contracture of toe Dimple chin Trismus Soft tissue sarcoma Impaired pain sensation Femoral hernia Hyponatremia Abnormality of digit Mesomelia Hyperkalemia Adrenal insufficiency Overlapping toe Metatarsus adductus Cutis marmorata Abnormality of dental morphology Unilateral renal agenesis Hammertoe Clitoral hypertrophy Proximal placement of thumb Precocious puberty Increased number of teeth Abnormality of the urinary system Reduced number of teeth Optic nerve hypoplasia Abnormality of the metacarpal bones Renal hypoplasia/aplasia Abnormal dermatoglyphics Hypercholesterolemia Holoprosencephaly Abnormality of dental enamel Hyperbilirubinemia Short toe Gingival overgrowth Biparietal narrowing Ulnar deviation of finger Amblyopia Sex reversal Advanced eruption of teeth Decreased circulating aldosterone level Hypocholesterolemia Abnormal localization of kidney Aplasia/Hypoplasia affecting the eye Abnormal renal morphology Gastrointestinal dysmotility Abnormality of the larynx Cholestatic liver disease Bicornuate uterus Bifid tongue Overlapping fingers Excessive daytime somnolence Aplasia/Hypoplasia of the radius Sclerocornea Severe failure to thrive Microglossia Male pseudohermaphroditism Postaxial foot polydactyly Self-mutilation Upper limb undergrowth Abnormal eyelash morphology Severe intrauterine growth retardation Abnormal lung lobation Epiphyseal stippling Hypopigmentation of hair Rhizomelia Abnormal form of the vertebral bodies Ectopic calcification Infantile muscular hypotonia Cerebellar hypoplasia Edema Hydrocephalus Intrauterine growth retardation Hypertension Cataract Abnormality of lower lip Hemifacial hypoplasia Macrodontia Language impairment Focal impaired awareness seizure Tented upper lip vermilion Sandal gap Polydactyly Generalized hirsutism Stereotypy Epileptic encephalopathy Short foot Highly arched eyebrow Small hand Downturned corners of mouth Synophrys Broad forehead Thin upper lip vermilion Coarse facial features Visual impairment Upslanted palpebral fissure Micropenis Split hand Peripheral demyelination Choanal atresia Cutaneous photosensitivity Renal hypoplasia Abnormality of the ribs Congenital diaphragmatic hernia Decreased fetal movement Oligohydramnios Ambiguous genitalia Eczema Narrow forehead Postaxial hand polydactyly Limb undergrowth Dandy-Walker malformation Proptosis Wide intermamillary distance Renal agenesis Webbed neck Intestinal malrotation Premature birth Postaxial polydactyly Pulmonary hypoplasia Micromelia Toe syndactyly Attention deficit hyperactivity disorder Low-set, posteriorly rotated ears Hypoglycemia Skeletal dysplasia Ureteropelvic junction obstruction Increased nuchal translucency Venous insufficiency Long face Coxa vara Wormian bones Coxa valga Narrow face Large fontanelles Recurrent urinary tract infections Cholestasis Blue sclerae Cerebral calcification Convex nasal ridge Bruising susceptibility Joint hypermobility Genu valgum Cutis laxa Narrow chest Platyspondyly Scarring Jaundice Pes planus Osteopenia Osteoporosis Hernia Renal insufficiency Dysphagia Skeletal muscle atrophy Recurrent pyelonephritis Osteolysis Coarse hair Fulminant hepatic failure Hiatus hernia Abnormality of fibula morphology Avascular necrosis of the capital femoral epiphysis Prominent superficial veins Broad ribs Generalized joint laxity Abnormality of the wrist Premature skin wrinkling Hypothermia Esophagitis Down-sloping shoulders Atypical scarring of skin Abnormality of the skull Carpal synostosis Hyperextensible skin Soft skin Short clavicles Acute kidney injury Short humerus Dislocated radial head Osteomalacia Orthostatic hypotension Limited elbow extension Delayed cranial suture closure Rickets Bilateral ptosis Redundant skin Hair-pulling Hyperorality Gastroschisis Facial capillary hemangioma Hepatic failure Unsteady gait Irritability Neonatal hypotonia Hyporeflexia Midface retrusion Headache Immunodeficiency Gait disturbance Cognitive impairment Elevated 7-dehydrocholesterol Abnormality of limbs Opsoclonus Full cheeks Severe photosensitivity Alveolar ridge overgrowth Septate vagina Abnormality of the gallbladder Hypoplasia of the frontal lobes Periventricular gray matter heterotopia Talipes calcaneovalgus Increased serum testosterone level Hip subluxation Median cleft palate Mesomelic short stature Broad alveolar ridges Thick vermilion border Renal dysplasia Cerebellar cortical atrophy Hypoplastic toenails Toenail dysplasia Episodic vomiting Periorbital fullness Delayed CNS myelination Concave nasal ridge Heat intolerance Arachnoid cyst Abnormality of the periventricular white matter Palpebral edema Poor eye contact Weak cry Cellulitis Large hands Nephrolithiasis Polycystic kidney dysplasia Prominent supraorbital ridges Recurrent upper respiratory tract infections Recurrent skin infections Poor head control Increased intracranial pressure Abnormality of the outer ear Sacral dimple Accelerated skeletal maturation Cerebral visual impairment Lymphedema Hypohidrosis Tall stature Aplasia/Hypoplasia of the cerebral white matter


If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like Frontal bossing and Thick vermilion border, related diseases and genetic alterations Motor delay and Single transverse palmar crease, related diseases and genetic alterations