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6,283 Possible Causes for Loss of Vision, No Polydactyly, Onset of Renal Dysfunction in Early Childhood

  • Alstrom Syndrome

    Sufferers often develop early-onset type 2 diabetes, renal and hepatic dysfunction affecting the liver and kidneys, bladder and bowel problems, and cardiomyopathy, where the[dailymail.co.uk] […] symptoms Cone Rod Dystrophy Sensorineural Hearing Loss Dilated Cardiomyopathy Obesity Insulin resistant Child 10-18 Lay terms Clinical terms Total loss of vision Not everyone[geneticdisordersuk.org] […] childhood, progressive neurosensory hearing loss, diabetes mellitus, acanthosis nigricans, hypogonadism with normal secondary sex characteristics, and kyphoscoliosis without polydactyly[ncbi.nlm.nih.gov]

  • Laurence Moon Syndrome

    We here present a case report of 18 year old male patient presenting in medicine department with weakness of both lower limbs, inability to walk, progressive loss of vision[ijmedph.org] Figure 2: showing polydactyly in lower limbs Figure 3: showing polydactyly in left hand Figure 4: showing high arched palate.[medresearch.in] Your child’s teacher of students with visual impairments should perform a functional vision assessment to determine how your child uses his or her vision in everyday life[familyconnect.org]

    Missing: Onset of Renal Dysfunction in Early Childhood
  • Retinitis Pigmentosa

    She presented with a history of acute, painless vision loss in her left eye over a period of 10 days.[ncbi.nlm.nih.gov] The two siblings showed signs of RP and polydactyly.[ncbi.nlm.nih.gov] […] are more likely to develop symptoms of RP earlier than those diagnosed with type two Laurence-Moon-Bardet-Beidl Syndrome – the symptoms of this syndrome can include RP, polydactyly[svrc.vic.edu.au]

    Missing: Onset of Renal Dysfunction in Early Childhood
  • Cortical Blindness

    In most cases, the complete loss of vision is not permanent and the patient may recover some of their vision (cortical visual impairment).[en.wikipedia.org] Homepage Rare diseases Search Search for a rare disease Cortical blindness-intellectual disability-polydactyly syndrome Disease definition A rare, genetic, multiple congenital[orpha.net] The main symptoms of this syndrome are rod-cone dystrophy (atypical retinitis pigmentosa), postaxial polydactyly, mental retardation, hypogonadism, and renal dysfunction ([journal.frontiersin.org]

    Missing: Onset of Renal Dysfunction in Early Childhood
  • Senior Loken Syndrome

    Early symptoms of the retinal dystrophy associated with Senior-Løken syndrome may include increased pigmentation (color) or loss of vision, and the inability to see at night[diseaseinfosearch.org] Physical examination should consider the presence of the main clinical signs of JSRD (hypotonia, ataxia and breathing abnormalities in infants) and BBS (polydactyly and obesity[orpha.net] Symptoms of RP range in age of onset and severity, and may include night blindness, progressive loss of peripheral vision, and eventual loss of central vision, leading to[rarediseases.info.nih.gov]

    Missing: Onset of Renal Dysfunction in Early Childhood
  • Retinitis

    A loss of side vision, or tunnel vision, is also common as RP progresses.[retinaspecialistsnw.com] The person having BBS also has extra fingers or toes a condition called polydactyly and hypogonadism, a condition affecting the secretion of hormones.[irisvision.com] Short stature, renal dysfunction, and polydactyly are some signs of Bardet-Biedl syndrome or Laurence-Moon syndrome when associated with pigmentary retinopathy.[patient.info]

    Missing: Onset of Renal Dysfunction in Early Childhood
  • Bardet-Biedl Syndrome Type 11

    Vision loss is one of the major features of Bardet-Biedl syndrome.[ghr.nlm.nih.gov] Polydactyly-type limb anomalies - these may be the only feature present at birth and are reported in 63-81% of patients.[patient.info] Your child’s teacher of students with visual impairments should perform a functional vision assessment to determine how your child uses his or her vision in everyday life[familyconnect.org]

    Missing: Onset of Renal Dysfunction in Early Childhood
  • Retinopathy

    If the disorder is severe, newborns require laser treatment, injections of bevacizumab, or surgery to prevent vision loss.[merckmanuals.com] Neuropathy, motor and sensory, Russe type (Charcot-Marie-Tooth disease type 4G) AD/AR 9 7 IDH3B Retinitis pigmentosa AR 2 3 IFT140 Short -rib thoracic dysplasia with or without polydactyly[blueprintgenetics.com] After 5 months of follow-up, this woman had had a normal delivery and her haemorrhages and vision loss had resolved.[ncbi.nlm.nih.gov]

    Missing: Onset of Renal Dysfunction in Early Childhood
  • Meckel Syndrome Type 7

    Hearing and vision loss may also occur. Lifespan is decreased.[natera.com] Keywords: Meckel-Gruber syndrome, occipital encephalocele, polycystic kidney, polydactyly How to cite this article: Panduranga C, Kangle R, Badami R, Patil PV.[ruralneuropractice.com] Keywords: M eckel Syndrome, Central Nervous System Malformations, Polydactyly and Hepatic Developmental Defects 1.[article.sciencepublishinggroup.com]

    Missing: Onset of Renal Dysfunction in Early Childhood
  • Branchio-Oculo-Facial Syndrome

    Dr.PALLAVI R PURPOSE To report a rare case of branchio oculo facial syndrome METHODS A 8yr old boy presented with loss of vision in left eye since birth.Ocular examination[proceedings.aios.org] This is only the second case where preaxial polydactyly has been described in branchio-oculo-facial syndrome.[ncbi.nlm.nih.gov] In addition to the structural differences, there can be visual impairment, hearing loss and speech disabilities.[rarediseases.org]

    Missing: Onset of Renal Dysfunction in Early Childhood

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