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12 Possible Causes for Progressive Prepubertal Onset Retinitis Pigmentosa

  • Usher Syndrome Type 1D

    USH1 is characterised by profound congenital sensorineural deafness, absent vestibular function and prepubertal onset of progressive retinitis pigmentosa leading to blindness[medical-dictionary.thefreedictionary.com] Usher Syndrome, Type IF [PCDH15]: Profound hearing loss and prepubertal onset of retinitis pigmentosa with progressive degeneration of the cells in the retina.[jewishgeneticdiseases.org] USH1 is characterized by profound congenital sensorineural deafness, absent vestibular function and prepubertal onset of progressive retinitis pigmentosa leading to blindness[genecards.org]

  • Autosomal Recessive Deafness 38

    USH1 is characterized by profound congenital sensorineural deafness, absent vestibular function and prepubertal onset of progressive retinitis pigmentosa leading to blindness[genecards.org]

  • Autosomal Recessive Deafness 23

    USH1 is characterized by profound congenital sensorineural deafness, absent vestibular function and prepubertal onset of progressive retinitis pigmentosa leading to blindness[genecards.org]

  • Usher Syndrome Type 1C
  • Usher Syndrome Type 1J

    USH1 is characterized by profound congenital sensorineural deafness, absent vestibular function and prepubertal onset of progressive retinitis pigmentosa leading to blindness[genecards.org] onset of progressive retinitis pigmentosa (RP).[centogene.com] […] near-normal, chance of later problem Usher syndrome type I (USH1) is the most severe form, characterized by severe to profound congenital deafness, vestibular areflexia, and prepubertal[centogene.com]

  • Usher Syndrome Type 1

    USH1 is characterised by profound congenital sensorineural deafness, absent vestibular function and prepubertal onset of progressive retinitis pigmentosa leading to blindness[medical-dictionary.thefreedictionary.com] USH1 is characterized by profound congenital sensorineural deafness, absent vestibular function and prepubertal onset of progressive retinitis pigmentosa leading to blindness[uniprot.org] onset of progressive retinitis pigmentosa (RP).[centogene.com]

  • Usher Syndrome Type 3B

    Usher Syndrome, Type IF [PCDH15]: Profound hearing loss and prepubertal onset of retinitis pigmentosa with progressive degeneration of the cells in the retina.[jewishgeneticdiseases.org] USH1 is characterized by profound congenital sensorineural deafness, absent vestibular function and prepubertal onset of progressive retinitis pigmentosa leading to blindness[genecards.org] onset of progressive retinitis pigmentosa (RP).[centogene.com]

  • Usher Syndrome

    USH1 is characterized by profound congenital sensorineural deafness, absent vestibular function and prepubertal onset of progressive retinitis pigmentosa leading to blindness[uniprot.org]

  • Usher Syndrome Type 2A

    onset of progressive retinitis pigmentosa (RP).[centogene.com] […] near-normal, chance of later problem Usher syndrome type I (USH1) is the most severe form, characterized by severe to profound congenital deafness, vestibular areflexia, and prepubertal[centogene.com]

  • Usher Syndrome 3A

    USH1 is characterised by profound congenital sensorineural deafness, absent vestibular function and prepubertal onset of progressive retinitis pigmentosa leading to blindness[medical-dictionary.thefreedictionary.com] onset of progressive retinitis pigmentosa (RP).[centogene.com] […] heterogeneous condition characterised by the association of retinitis pigmentosa and sensorineural deafness; the clinical forms—USH1, USH2 and USH3—are distinguished based on age at onset[medical-dictionary.thefreedictionary.com]

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