Phenotypes for disease #05716 (KFSD (keratosis follicularis spinulosa decalvans (KFDS)), OMIM:612843)

5 entries on 1 page. Showing entries 1 - 5.
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0000352023 keratosis follicularis spinulosa decalvans KFSDX see paper; ..., normal birth, low birth weight (2,700g), small placenta, thin maternal cord; erythroderma, collodion membrane, scaling skin, facial erythema, hypohidrosis, non-cicatricial alopecia totalis, absent eyelashes, photophobia; 11m-non-specific febrile seizures, generalized hypohidrosis Isolated (sporadic) 00y11m - - - Johan den Dunnen 00466659
0000352024 keratosis follicularis spinulosa decalvans KFSDX see paper; ..., birth little hair, rough skin; 1y-no scalp hair; 20y-complete alopecia, no eyebrows, no eyelashes, dry skin, widespread follicular papules, normal teeth, no intellectual disability, no photophobia performance Familial, X-linked recessive 20y - - - Johan den Dunnen 00466660
0000352025 keratosis follicularis spinulosa decalvans KFSDX see paper; ..., mild photophobia; angular cheilitis, dystrophic nails, no scalp hair, no eyebrows, no eyelashes, spiky follicular hyperkeratosis predominantly on scalp and extensor surfaces extremities;normal hearing, normal vision, normal growth development, no intellectual disability Unknown 06y - - - Johan den Dunnen 00466661
0000352029 keratosis follicularis spinulosa decalvans KFSDX see paper; ..., 6m-loss of eyebrows, roughness skin; marked loss both eyebrows, erythema, perifollicular accentuation,follicular hyperkeratosis, Familial, X-linked recessive 00y06m - - - Johan den Dunnen 00466666
0000352075 keratosis follicularis spinulosa decalvans - see paper; ..., generalised follicular hyperkeratosis, dry skin, scarring alopecia scalp, sparse eyebrows, sparse eyelashes, occipital folliculitis, hypohidrosis, myopia, astigmatism Familial, autosomal dominant 31y - - - Johan den Dunnen 00466712
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