Disease Comparison Results (show all mode) for Klipple-Feil syndrome and Pallister W Syndrome

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Pallister W Syndrome

Found: 52 | Differences: 34

Klipple-Feil syndrome

Found: 70 | Differences: 52

Klipple-Feil syndrome and Pallister W Syndrome sharing 18 common findings. (show all, show common, show differences)

Clinical Manifestations
Signs & Symptoms
Particular physiognomy/Odd looking kids
Broad flat nose/facies
Craniofacial Abnormalities/Congenital
Face broad/flat midface
Facies particular
Midfacial hypoplasia/flat face dysmorphism
Uvula anomaly/deformity
Delayed speech/language development
Infant Seizures
Mental Deficiency Child
Seizures
Seizures/Children/recurrent
Delayed speech development/impediment
Snoring
Dysmorphic appearance/face
Downward sloping eyes/Antimongoloid slant
Clinical Presentation & Variations
Presentation/Multiple deformities newborn (odd look)
Disease Progression
Course/Chronic disorder
Course/Chronic only
Demographics & Risk Factors
Population Group
Child
Population/Pediatrics population
Family History
Family history/Skeletal malformations
Sex & Age Groups
Population/Child
Population/Child-Infant Only
Population/Children/all
Associated Diseases & Rule outs
Associated Disease & Complications
Cleft Lip
Cleft lip/deformity
Cleft palate/deformity
Convulsions (grand mal)
Epilepsy
Hypertelorism/Wide Spaced Eyes
Mental retardation
Pallister W Syndrome
Skeletal dysplasia
Skeletal/bone malformations
Disease Mechanism & Classification
Class
CLASS/Pediatric disorders (ex)
CLASS/Long bone involvement/disorder (ex)
Pathophysiology
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Maternal Chromosome mutation
Process
PROCESS/Congenital/developmental (category)
PROCESS/Eponymic (category)
PROCESS/Eponymic/Esoteric/Not yet integrated into database
PROCESS/Genetic disorder/Spontaneous mutations/sporadic
PROCESS/Hereditofamilial (category)
PROCESS/INCIDENCE/Esoteric disease (example)
PROCESS/INCIDENCE/Extremely rare disease
PROCESS/Multiple dysmorphic syndrome (ex)
PROCESS/Anomalies/Deformities/Malformations (EX)
PROCESS/Dystostosis/craniofacial (ex)
Synonyms
Synonym
Synonym/W Syndrome
Clinical Manifestations
Signs & Symptoms
Congenital low hairline
Facial Asymmetry
Short neck/Brevicollis
Webbed neck deformity/Broad neck
Difficulty flexing neck
Headache in children
Asymmetric Limbs
Cervical kyphosis sign
Cervical spine/neck limited motion
Macrocephaly/Large head
Megalocephaly
Spine pain/vertebral skeletal pain
Upper back skeletal deformity/signs
Difficult intubations/anatomic
Snoring
Lateral Asymmetry
Moves head to see/not eyes/stiff collar look
Disease Progression
Course/Chronic disorder
Course/Chronic only
Demographics & Risk Factors
Population Group
Child
Population/Pediatrics population
Sex & Age Groups
Population/Child
Population/Child-Infant Only
Population/Children/all
Diagnostic Test Results
X-RAY
Xray/Anomalous rib cage/congenital
Xray/Ribs Abnormal/Deformities
Xray/Spine Abnormal
Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs
Turner syndrome
Associated Disease & Complications - Causes
Atrial septal defect
Coarctation of aorta
Congenital urinary tract malformations
Congenitally fused cervical vertebrae
Deafness
Deafness, congenital
Fused Neck Vertebrae Anomalies
Hemivertebrae Neck Anomalies
Klippel-Feil syndrome
Kyphoscoliosis
Kyphosis
Obstructive sleep apnea/Children
Platybasia
Renal anomalies
Rib anomalies/Hypoplastic/deformed
Skeletal dysplasia
Skeletal/bone malformations
Sprengel deformity
Thoracic deformity/congenital
Torticollis, acquired
Torticollis, congenital
Vertebrae Anomalies
Torticollis
Disease Mechanism & Classification
Class
CLASS/Pediatric disorders (ex)
CLASS/Axial skeletal involvement/disorder (ex)
CLASS/Skeletal (category)
CLASS/Vertebra/Spine disorder (ex)
Pathophysiology
Pathophysiology/Asymmetric deformities
Pathophysiology/Gene Locus Identified/OMIM database
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Sporadic/hereditary/process
Pathophysiology/Maternal Chromosome mutation
Pathophysiology/Gene locus 8q22.2-q23.3
Pathophysiology/Gene locus chromosome 8
Process
PROCESS/Autosomal dominant hereditary disease (ex).
PROCESS/Autosomal recessive disorder (ex)
PROCESS/Congenital/developmental (category)
PROCESS/Eponymic (category)
PROCESS/Genetic disorder/Spontaneous mutations/sporadic
PROCESS/Hereditofamilial (category)
PROCESS/Anomalies/Deformities/Malformations (EX)
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