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180 Possible Causes for Cornea, Male Sterility, Prader-Willi Syndrome

  • Laurence Moon Syndrome

    Grand father had polydactyly, aunt (father's sister) had polydactyly with sterility.[] CORNEA GUTTATA DISTROFIA COMBINATA DELLA CORNEA DISTROFIA ENDOTELIALE DI FUCHS DISTROFIA CORNEALE ENDOTELIALE POSTERIORE POLIMORFA RF0280 CHERATOCONO RF0290 CONGIUNTIVITE[] 】 多腺性自己免疫症候群 【 polyuria 】 多尿 【 Prader-Willi syndrome 】 プラダー・ウィリー症候群 【 primary aldosteronism 】 原発性アルドステロン症 【 progesterone 】 プロゲステロン 【 prolactin (PRL) 】 プロラクチン 【 prolactinoma[]

  • Prader-Willi Syndrome

    In 1976, physicians became aware that Creutzfeldt–Jakob disease could be transmitted by neurosurgical procedures and cornea transplantation.[] Prader-Labhart-Willi syndrome PWS Willi-Prader syndrome Bittel DC, Butler MG. Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology.[] Prader-Willi Syndrome. 1998 Oct 6 [updated 2016 Feb 4].[]

  • Hypogonadism

    […] aging male, Fertility and Sterility, 10.1016/j.fertnstert.2008.08.094, 90, 5, (S83-S87), (2008).[] Gokcen Gokce, Volkan Hurmeric, Tarkan Mumcuoglu, Gokhan Ozge, Yalcin Basaran, Hilmi Umut Unal, Erol Bolu and Fatih Mehmet Mutlu, Effects of androgen replacement therapy on cornea[] ., Klinefelter syndrome, hemochromatosis, Kallmann syndrome, Prader-Willi syndrome, and mytonic dystrophy) can also cause low testosterone.[]

  • Monosomy 6p23

    sterility due to Y-chromosome deletions Monosomy 7 of Bone Marrow NF1 Microdeletion Syndrome Otodental Dysplasia Potocki-Shaffer syndrome Prader-Willi-Like Syndrome Associated[] Usually the involvement is limited to the peripheral part of the cornea but it may extend to the entire cornea, so-called sclerocornea totalis.[] - W 15q11.2-q13.1 Angelman-Syndrom Typ1 Microdup. 15 Syndrom D/LL 15q11.2-q13.1 Angelman-Syndrom Typ2 Microdup. 15 Syndrom D/LL 15q11.2-q13.1 Prader-Willi- Syndrom Typ 1[]

  • Panhypopituitarism

    Secondary infections: the inflammation of the uveal tract due to its spread from other ocular tissues- cornea, sclera or retina.[] Bardet-Biedl syndrome and Prader-Willi syndrome have been associated with pituitary hormone deficiencies.[] […] deficiency ("CPHD") include: Type OMIM Gene CPHD1 613038 POU1F1 CPHD2 262600 PROP1 CPHD3 600577 LHX3 CPHD4 602146 LHX4 CPHD5 (Septo-optic dysplasia) 182230 HESX1 Kallmann syndrome[]

  • Neuhauser Syndrome

    Fertil Steril 63: 1326–1328 PubMed Google Scholar Koeppen AH (1998) The hereditary ataxias.[] Ophthalmologic examination demonstrated central opacity of the left cornea and lens and iris adhesions extending from the pupillary margin to the borders of the opacity.[] This pathogenesis exists in some hypothalamic dysfunctions, such as Kallmann syndrome or Prader-Willi syndrome.[]

  • Noonan Syndrome

    […] experience infertility (sterility).[] Br J Ophthalmol 1987, 71 : 235–8. 19 Bleshoy H : Sensitivity and neuropathology in the Keratoconic Cornea: PHD. City University, Northampton Square, London. 1990.[] Prader-Willi Syndrome What is Prader-Willi syndrome? Prader-Willi syndrome (PWS) is a rare genetic disorder that affects both boys and girls.[]

  • Autosomal Dominant Mental Retardation Type 21

    Possible dextrocardia, male sterility. Pyruvate Dehydrogenase Deficiency Autosomal Recessive.[] The first signs of AAK appear in the first decade of life, with thickening and vascularization of the peripheral cornea, which gradually advances into the central cornea,[] ., paternal del(15)(q11.2q13) in Prader-Willi syndrome and maternal del(15)(q11.2q13) in Angelman syndrome).[]

  • Laron Syndrome with Immunodeficiency

    Autosomal recessive nonsyndromic deafness Autosomal recessive non-syndromic sensorineural deafness type DFNB 1 0 Deafness-infertility syndrome Deafness, sensineural, and male[] CORNEA GUTTATA DISTROFIA COMBINATA DELLA CORNEA DISTROFIA ENDOTELIALE DI FUCHS DISTROFIA CORNEALE ENDOTELIALE POSTERIORE POLIMORFA DISTROFIA CORNEALE EPITELIALE GIOVANILE[] DUE TO A POINT MUTATION Is also known as schaaf-yang syndrome pws due to a point mutation pwls prader-willi-like syndrome Related symptoms: Intellectual disability Seizures[]

  • Autosomal Recessive Congenital Cataract 5

    Possible dextrocardia, male sterility. Pyruvate Dehydrogenase Deficiency Autosomal Recessive.[] Causes of congenital corneal opacities may be classified as primary corneal disease or secondary corneal disease.[] Similar to and more severe than Edward's Syndrome. Death by 1 year old. Prader-Willi Syndrome Chromosomal Deletion of part of short arm of chromosome 15, paternal copy.[]