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1,312 Possible Causes for Cataract, Ichthyosis, Xeroderma

  • Ichthyosis Vulgaris

    PLATANUS OCCIDENTALIS 30 —Platanus occidentalis is prescribed for X linked ichthyosis with corneal opacity and cataract.[ks-gopi.blogspot.com] Bathing suit ichthyosis or congenital ichthyosis, due to an autosomal recessive gene, is characterized by the presence of scaly skin on the bathing suit areas but not on the[symptoma.com] […] disease Common ichthyosis ICHTHYOSIS VULGARIS edit English ichthyosis vulgaris skin disorder causing dry, scaly skin.[wikidata.org]

  • Ichthyosis

    In a third in which the mother had cataracts and ichthyosis, two of her female children had cataracts.[disorders.eyes.arizona.edu] Ichthyosis, also called fish-skin disease, or xeroderma, a hereditary condition involving dryness and scaliness of the skin brought about by excessive growth of the horny[britannica.com] There are 5 major types of IT: Ichthyosis vulgaris (the most common of the five), recessive X-linked ichthyosis, autosomal recessive congenital ichthyosis-1 (ARCI1), keratinopathic[symptoma.com]

  • Atopic Dermatitis

    After routine cataract surgery, the anterior subcapsular cataractous tissue was obtained as an anterior capsulorhexis flap and prepared as a wholemount for histological analysis[ncbi.nlm.nih.gov] Particularly, xeroderma pigmentosum patients are characterized by a 1,000-fold increased susceptibility to sunlight-induced skin cancer ( 4 ).[doi.org] Recognize ichthyosis vulgaris and know that ichthyosis commonly occurs in children who have atopic dermatitis.[pedsinreview.aappublications.org]

  • Cerebro-Oculo-Facio-Skeletal Syndrome Type 1

    Cerebro-oculo-facio-skeletal (COFS) syndrome is a rapidly progressive neurological disorder leading to brain atrophy with calcification, cataracts, microcornea, optic atrophy[ncbi.nlm.nih.gov] Inherited defects in NER result in profound photosensitivity and the cancer-prone syndrome xeroderma pigmentosum (XP) or two progeroid syndromes: Cockayne and trichothiodystrophy[ncbi.nlm.nih.gov] ichthyosis on his face, trunk and limbs.[ncbi.nlm.nih.gov]

  • Tricho-Retino-Dento-Digital Syndrome

    Nails Hair Hair: pili canaliculi uncombable hair pili trianguli Genitourinary External Genitalia Male: hypospadias Skeletal Feet: brachydactyly Head And Neck Eyes: juvenile cataract[malacards.org] […] hypohidrotic dysplasia Tricho retino dento digital syndrome Tricho-dento-osseous syndrome Tricho-hepato-enteric syndrome Trichodermodysplasia dental alterations Trichodysplasia xeroderma[mindmappedia.com] […] abnormalities Autosomal ichthyosis syndrome with prominent neurologic signs Autosomal recessive congenital ichthyosis Autosomal recessive cutis laxa type 1 Autosomal recessive[se-atlas.de]

  • Spondyloepimetaphyseal Dysplasia-Hypotrichosis Syndrome

    The ectodermal traits are clearly seen as trichodysplasia, onychodysplasia, skin manifestations, and nuclear cataract.[docslide.com.br] […] pigmentosum, group A XPA Xeroderma pigmentosum, group C XPC Xeroderma pigmentosum, group D ERCC2 Xeroderma pigmentosum, group E, DDB-negative subtype DDB2 Xeroderma pigmentosum[centogene.com] Nervous system disease H00733 Harlequin ichthyosis Harlequin ichthyosis (HI) is the most devastating form of congenital ichthyosis.[kegg.jp]

  • CAMFAK Syndrome

    Diseases related to Cataract, Microcephaly, Failure to Thrive, Kyphoscoliosis Syndrome via text searches within MalaCards or GeneCards Suite gene sharing: Human phenotypes[malacards.org] He is also the Editor of Molecular Mechanisms of Fanconi Anaemia, Molecular Mechanisms of Xeroderma Pigmentosum, Molecular Mechanisms of Ataxia Telangiectasia and Molecular[books.google.com] […] skeletal anomalies Juvenile retinoschisis Deafness, epiphyseal dysplasia, short stature Angioma hereditary neurocutaneous Mucopolysaccharidosis type IIIC Macrozoospermia Ichthyosis[checkrare.com]

  • Keratitis Bullosa

    Cornea and cataract. In: Emery, J.M.[link.springer.com] […] ou) Corneal Vascularisation DOUBLE PTERYGIUM OF LEFT EYE Melanin Granules on Corneal Endothelium (Krukenberg Spindle), (Colour Photography, OCT) Peripheral Degenerations Xeroderma[atlasophthalmology.net] […] ichthyosiform erythroderma, ichthyosis vulgaris, and X-linked ichthyosis).[firstskinfoundation.org]

  • Congenital Ichthyosis

    […] delayed neuromuscular development and other CNS anomalies, dysplasia of nails, hypoplasia of subcutaneous fatty tissue, prematurely aged facial appearance, hypogonadism, cataracts[ncbi.nlm.nih.gov] Also called fish skin disease, xeroderma. ichthyotic, adj.[medical-dictionary.thefreedictionary.com] The various types of congenital ichthyosis are usually diagnosed at birth, based on the characteristic appearance of the newborn.[symptoma.com]

  • Hereditary Mucoepithelial Dysplasia

    A 16-year-old patient had nontender, fire-red mucosae; keratosis pilaris; diffuse, nonscarring alopecia; cataracts; photophobia; corneal vascularization; and decreased visual[ncbi.nlm.nih.gov] […] and Hospital & The Tamilnadu Dr.MGR Medical University Published on Mar 14, 2017 Ectodermal Dysplasia White Sponge Nevus Hereditary Benign Intraepithelial Dyskeratiosis Xeroderma[slideshare.net] Ohkawara, Ichthyosis follicularis with alopecia and photophobia in a mother and daughter, British Journal of Dermatology, 142, 1, (157), (2000).[doi.org]

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