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4,913 Possible Causes for Cataract, Occasional Hypogonadism, Prominent High Nasal Root

  • Noonan Syndrome

    He underwent an eye examination after complaining of decreased visual acuity in the right eye and was diagnosed with mature cataract, which was treated by cataract surgery[ncbi.nlm.nih.gov] The triangular facial features become even sharper in teenagers and young adults, with a pinched root and a thin, high bridge on the nose.[touchendocrinology.com] During adolescence, the nasal bridge is thinner and higher, with a “pinched” root and wide base, and the eyes appear less prominent.[rarediseases.org]

  • Hallermann-Streiff Syndrome

    To report two cases of Hallermann-Streiff syndrome with exudative retinal detachment after cataract surgery. Case report.[ncbi.nlm.nih.gov] nasal bridge Elevated nasal bridge High nasal bridge Prominent bridge of nose Prominent nasal root Protruding bridge of nose Protruding nasal bridge [ more ] 0000426 Pulmonary[rarediseases.info.nih.gov] Ophthalmic abnormalities included bilateral congenital cataract. Glaucoma is uncommon.[ncbi.nlm.nih.gov]

    Missing: Occasional Hypogonadism
  • Rothmund Thomson Syndrome

    About 40% of adult patients show delayed puberty or hypogonadism.[plasticsurgerykey.com] […] human disease Congenital poikiloderma RTS Rothmund-Thomson syndrome (disorder) ROTHMUND-THOMSON SYNDROME Poikiloderma Atrophicans and Cataract ROTHMUND-THOMSON SYNDROME; RTS[wikidata.org] Recently we encountered a 25-year-old white woman who had developed this syndrome but without juvenile cataracts, hypogonadism, or mental retardation.[ncbi.nlm.nih.gov]

    Missing: Prominent High Nasal Root
  • Congenital Cataract

    Note that cataract may affect one or both eyes.[symptoma.com] We present a Hungarian girl with microcephaly, microphthalmia, congenital cataract, prominent nasal root, peaked nose, micrognathia with high arched palate, mild mental retardation[ncbi.nlm.nih.gov] From Wikidata Jump to navigation Jump to search disorder of lens edit Language Label Description Also known as English Congenital cataract disorder of lens Statements subclass[wikidata.org]

    Missing: Occasional Hypogonadism
  • Schwartz-Jampel Syndrome

    Ocular manifestation is a part of the syndrome and include blepharospasm, cataract, subluxation of lens and myopia.[ajol.info] nasal bridge Elevated nasal bridge High nasal bridge Prominent bridge of nose Prominent nasal root Protruding bridge of nose Protruding nasal bridge [ more ] 0000426 Ptosis[rarediseases.info.nih.gov] […] developmental, eye, genetic, neurological Phenotypes Abnormality of femoral epiphysis ; Anterior bowing of long bones ; Autosomal recessive inheritance ; Blepharophimosis ; Cataract[mousephenotype.org]

    Missing: Occasional Hypogonadism
  • Chudley-Rozdilsky Syndrome

    Microcornea Syndrome Cataract, Microcephaly, Arthrogryposis, Kyphosis Syndrome Cataracts, Ataxia, Short Stature, and Mental Retardation Catel Manzke Syndrome Cauda equina[rgd.mcw.edu] nasal bridge Elevated nasal bridge High nasal bridge Prominent bridge of nose Prominent nasal root Protruding bridge of nose Protruding nasal bridge [ more ] 0000426 Protruding[rarediseases.info.nih.gov] Muscular dystrophy, congenital, infantile with cataract and hypogonadism 0 *Cataract *Hypogonadism *Muscular Dystrophies/congenital.[reference.md]

    Missing: Occasional Hypogonadism
  • Warburg Micro Syndrome 3

    Differential diagnosis Micro syndrome should be considered in any infant with congenital cataract.[rarediseases.info.nih.gov] Hypogonadotropic hypogonadism leads to cryptorchidism, micropenis, labioscrotal fusion, and hypoplastic scrotum.[iamg.in] She presented with bilateral microphthalmia and cataract at birth.[cags.org.ae]

    Missing: Prominent High Nasal Root
  • CAMFAK Syndrome

    Hypogonadotropic hypogonadism leads to cryptorchidism, micropenis, labioscrotal fusion, and hypoplastic scrotum.[iamg.in] Diseases related to Cataract, Microcephaly, Failure to Thrive, Kyphoscoliosis Syndrome via text searches within MalaCards or GeneCards Suite gene sharing: Human phenotypes[malacards.org] Related Pathways Cataract, Microcephaly, Failure To Thrive, Kyphoscoliosis Syndrome has been linked to: Pathogenesis Alternate Names Cataract, Microcephaly, Failure To Thrive[novusbio.com]

    Missing: Prominent High Nasal Root
  • Hypergonadotropic Hypogonadism-Cataract Syndrome

    However, a hypergonadotropic hypogonadism is occasionally seen in patients with neurological dis- orders.[myslide.es] You are donating to research for a rare disease: ' Hypergonadotropic hypogonadism - cataract syndrome '.[react-community.org] Less common clinical manifestations Hypergonadotropic hypogonadism (primary hypogonadism) Type 1 diabetes mellitus Autoimmune thyroid disease (not including Graves disease[emedicine.medscape.com]

    Missing: Prominent High Nasal Root
  • Woodhouse Sakati Syndrome

    […] sensorineural hearing impairment Choreoathetosis Decreased serum estradiol Decreased serum testosterone level Decreased testicular size Dysarthria Dystonia Hypergonadotropic hypogonadism[dovemed.com] […] epilepsy Hutterite cerebroosteonephrodysplasia syndrome Ayazi syndrome Male pseudohermaphroditism due to defective LH molecule Omenn syndrome Early-onset anterior polar cataract[checkrare.com] nasal bridge Elevated nasal bridge High nasal bridge Prominent bridge of nose Prominent nasal root Protruding bridge of nose Protruding nasal bridge [ more ] 0000426 Prominent[rarediseases.info.nih.gov]

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