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Disease Comparison Results (show all mode) for Facial ectodermal dysplasia (Setleis) and Leprechaunism

Clinical
Demographics
Diagnostic
Diseases
Classification
Synonyms
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Found: 41 | Differences: 20

Found: 72 | Differences: 51

Facial ectodermal dysplasia (Setleis) and Leprechaunism sharing 21 common findings. (show all, show common, show differences)

Clinical Manifestations
Signs & Symptoms: Particular physiognomy/Odd looking kids; Craniofacial Abnormalities/Congenital; Facies particular; Nipple enlargement; Hirsutism; Idiocy/signs; Mental Deficiency Child; Clitoral enlargement; Dysmorphic dwarfism/short stature; Dysmorphic appearance/face; Short stature; Short stature Child
Clinical Presentation & Variations: Presentation/Multiple deformities newborn (odd look); Presentation/Kidney malformations Congenital syndrome Child
Disease Progression: Course/Chronic disorder; Course/Chronic only; Course/Lethal

Demographics & Risk Factors
Population Group: Child; Infant; Population/Pediatrics population
Family History: Family history/Parental consanguinity
Sex & Age Groups: Population/Child; Population/Child-Infant Only; Population/Children/all; Population/Female; Population/Girl patient; Population/Infant; Population/Infant female

Diagnostic Test Results
X-RAY: Xray/Retarded skeletal maturation

Associated Diseases & Rule outs
Associated Disease & Complications: Hypoglycemia; Mental retardation

Disease Mechanism & Classification
Class: CLASS/Pediatric disorders (ex); CLASS/Systemic/no comment (category)
Pathophysiology: Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Process: PROCESS/Autosomal recessive disorder (ex); PROCESS/Congenital/developmental (category); PROCESS/Hereditofamilial (category); PROCESS/INCIDENCE/Rare disease (ex); PROCESS/Multiple dysmorphic syndrome (ex); PROCESS/Dystostosis/craniofacial (ex)

Synonyms
Synonym: Synonym/Donohue's syndrome

Clinical Manifestations
Signs & Symptoms: Loose facial skin/rubbery look; Particular physiognomy/Odd looking kids; Bulbous nose/congenital; Congenital facial deformities; Craniofacial Abnormalities/Congenital; Facies particular; Leonine Facies/Jowles; Mongoloid Facies; Prominent lips; Prominent Nose; Short upper lip; Wide Nasal Bridge; Bitemporal circular depressions/scars congenital; Excess loose skin/child; Hypopigmentation; Increased pigmentation/tanning/hyperpigmented; Increased wrinkling/skin; Pigmented/skin folds/flexor/palmar creases; Scalp hair sparse/thin; Sparse hair distribution/Hypotrichosis; Carious teeth/child; Carious teeth/sign; Scarlike median ridge chin; Teeth malformed/dysplastic; Psychomotor retardation; Snoring; Dysmorphic appearance/face; Abnormal double row eyelashes; Bilateral Eyelid Edema; Infra-orbital skin creases; Mongoloid eye slant/congenital/sign; Periorbital edema/Puffy eyes
Clinical Presentation & Variations: Presentation/Multiple deformities newborn (odd look); Presentation/Infant Loose redundant skin Face no eyelashes
Disease Progression: Course/Chronic disorder; Course/Chronic only

Demographics & Risk Factors
Population Group: Child; Infant; Population/Pediatrics population
Sex & Age Groups: Population/Child; Population/Child-Infant Only; Population/Children/all; Population/Female; Population/Infant

Associated Diseases & Rule outs
Associated Disease & Complications: Congenital anomalies; Dental caries; Dental deformities/anomalies; Facial dysplasia; Hyperpigmentation; Multiple Congenital Anomalies; Multiple congenital anomalies/Mental retardation; Teeth enamel hypoplastic

Disease Mechanism & Classification
Class: CLASS/Jablonski/NIH Archive Anomalies Database; CLASS/Pediatric disorders (ex); CLASS/Dermatologic/Subcutaneous (category); CLASS/Hair involvement/disorder (ex)
Pathophysiology: Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations); Pathophysiology/Subcutaneous manifestation/involvement; Pathophysiology/Maternal Chromosome mutation
Process: PROCESS/Autosomal dominant hereditary disease (ex).; PROCESS/Autosomal recessive disorder (ex); PROCESS/Eponymic (category); PROCESS/Genetic disorder/Spontaneous mutations/sporadic; PROCESS/Genetic expressivity variable (ex); PROCESS/Hereditofamilial (category); PROCESS/INCIDENCE/Extremely rare disease; PROCESS/INCIDENCE/Rare disease (ex); PROCESS/Dystostosis/craniofacial (ex)

Synonyms
Synonym: Synonym/Bitemporal forceps marks syndrome; Synonym/FFDD type II; Synonym/Focal facial dermal dysplasia type II; Synonym/Setleis syndrome

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