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4 Possible Causes for Allelic Disorder to IFAP Syndrome, Large Upper Right Central Incisor

  • X-Linked Keratosis Follicularis Spinulosa Decalvans

    IFAP syndrome is an allelic disorder, being genotypically and phenotypically similar to KFSD.[] Anteversion of the upper anterior teeth, congenital absence of right lower central incisors, and deep overbite and overjet of the anterior teeth also were seen.[] ) syndrome and Graham Little Piccardi Lasseur syndrome (GLPLS).[]

  • Autosomal Dominant Prognathism

    Examination of oral cavity revealed several deciduous teeth without any upper right permanent central incisor or lower permanent central incisor.[] Panoramic X-ray revealed a large number of unerupted permanent teeth, residual baby teeth, and several supernumerary impacted teeth ( Fig. 4 ).[]

    Missing: Allelic Disorder to IFAP Syndrome
  • Atrophodermia Vermiculata

    See also IFAP syndrome (308205), an allelic disorder with an overlapping phenotype.Keratosis follicularis spinulosa decalvans is an uncommon genodermatosis chiefly characterized[] disorder to IFAP syndrome (308205) MOLECULAR BASIS: Caused by mutation in the membrane-bound transcription factor protease, site 2 gene (MBTPS2, 300294.0006) Keratosis (from[] ; Scarring alopecia; Sparse eyelashes; Sparse eyebrows MISCELLANEOUS: Genetic heterogeneity; Onset in infancy or early childhood; Carrier females may have mild features; Allelic[]

    Missing: Large Upper Right Central Incisor
  • Autosomal Dominant Mental Retardation Type 5

    […] and lower lateral incisors; Large upper right central incisor; Overlapping left central incisor CHEST: [Diaphragm]; Right diaphragmatic hernia (rare) SKELETAL: [Hands]; Pedunculated[] Posteriorly rotated ears; Hearing loss, unilateral, mild; [Eyes]; Ptosis, bilateral; Hypertelorism; Exophthalmos, mild; Downslanting palpebral fissures; [Teeth]; Absence of upper[]

    Missing: Allelic Disorder to IFAP Syndrome

Further symptoms