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680 Possible Causes for coucher, Rieger Syndrome

  • Glaucoma

    Rhee -- Primary congenital glaucoma -- Glaucoma associated with congenital anomalies -- Aniridia -- Axenfeld's anomaly -- Rieger's anomaly -- Rieger's syndrome -- Peter's[worldcat.org] Clinical syndromes -- Introduction to clinical syndromes / Douglas J. Rhee -- Developmental glaucomas (congenital glaucomas) / Oscar V.[worldcat.org]

    Missing: coucher
  • SHORT Syndrome

    Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome. Nat Genet 1996; 14:392-399. ‏[books.google.com] Robert James Gorlin (born 1923), et al: Rieger anomaly and growth retardation (the S-H-O-R-T syndrome).[whonamedit.com] Methods: : A pedigree comprising 3 individuals affected by Axenfeld-Rieger syndrome, glaucoma and short stature was ascertained.[iovs.arvojournals.org]

    Missing: coucher
  • Rieger Syndrome

    : Axenfeld-Rieger Syndrome, Type 2, also known as axenfeld-rieger syndrome type 2 , is related to axenfeld-rieger syndrome, type 3 and axenfeld-rieger syndrome .[malacards.org] 症候群 Type 1 Axenfeld-Rieger Syndrome Type 1 Rieger Syndrome Type 3 Axenfeld-Rieger Syndrome Type 3 Rieger Syndrome アクセンフェルト・リーガー症候群 アクセンフェルド・リーガー症候群 リーガー奇形 リーガー症候群 解説語: 関連語[lsd-project.jp] (DO) Axenfeld-Rieger syndrome type 3 Brachymetapody-Anodontia-Hypotrichosis-Albinoidism Cleft Palate, Deafness, and Oligodontia Deafness Oligodontia Syndrome Dermatoosteolysis[rgd.mcw.edu]

    Missing: coucher
  • Familial Partial Lipodystrophy

    Abstract Familial lipodystrophy (referred to in publications as the Köbberling-Dunnigan syndrome) comprises at least two clinical phenotypes which are consistent within each pedigree. In type 1 familial lipodystrophy, loss of subcutaneous fat is confined to the limbs, sparing the face and trunk. In type 2 familial[…][ncbi.nlm.nih.gov]

    Missing: coucher
  • Contusion of Eye and Adnexa

    Born in Samsun in 1960, Gungor Sobaci graduated from Kuleli Military High School, Istanbul in 1977 and from Ankara University Medical School in 1983. He was then appointed as lieutenant medical doctor in the 7th Army Corps Headquarters in Diyarbakir for 2.5 years. After completing a 6-month advanced English Course in[…][books.google.de]

    Missing: coucher
  • Axenfeld-Rieger Syndrome Type 3

    Axenfeld Anomaly AXENFELD-RIEGER SYNDROME, TYPE 3 Rieger Syndrome, Type 3 Axenfeld-Rieger Anomaly Rieger Anomaly AXENFELD-RIEGER SYNDROME, TYPE 3; RIEG3 edit English Axenfeld-Rieger[wikidata.org] More Symptoms of Axenfeld-Rieger syndrome type 3 » Types of Axenfeld-Rieger syndrome type 3 Some types of this condition may include: 2 Types of Axenfeld-Rieger syndrome type[familydiagnosis.com] 症候群 Type 1 Axenfeld-Rieger Syndrome Type 1 Rieger Syndrome Type 3 Axenfeld-Rieger Syndrome Type 3 Rieger Syndrome アクセンフェルト・リーガー症候群 アクセンフェルド・リーガー症候群 リーガー奇形 リーガー症候群 解説語: 関連語[lsd-project.jp]

    Missing: coucher
  • Axenfeld Syndrome

    Term Name: Axenfeld-Rieger syndrome type 3 Search Ontology: Synonyms: anterior chamber cleavage syndrome anterior segment mesenchymal dysgenesis Axenfeld-Rieger anomaly with[zfin.org] Axenfeld syndrome RGS - Rieger syndrome Rieger's anomaly Hagedoom syndrome edit English Axenfeld-Rieger syndrome autosomal dominant disease characterized by abnormalities[wikidata.org] 症候群 Type 1 Axenfeld-Rieger Syndrome Type 1 Rieger Syndrome Type 3 Axenfeld-Rieger Syndrome Type 3 Rieger Syndrome アクセンフェルト・リーガー症候群 アクセンフェルド・リーガー症候群 リーガー奇形 リーガー症候群 解説語: 関連語[lsd-project.jp]

    Missing: coucher
  • Axenfeld Anomaly

    […] of the heterogeneous disorder termed Axenfeld-Rieger Syndrome (ARS).[books.google.ro] Axenfeld-Rieger Syndrome, Type 3 Clinical Characteristics Ocular Features: The most important ocular feature is glaucoma, found in greater than 50% of patients.[disorders.eyes.arizona.edu] Length: 17 minutes 40 seconds Chapter: Axenfeld-Rieger Syndrome, Peter anomaly Version: 1.0 Description: This is version 1.0. Notes on any changes will be added here.[curriculum.iowaglaucoma.org]

    Missing: coucher
  • Peters Anomaly

    One patient had Axenfeld anomaly, one had Rieger syndrome, and one had both Axenfeld anomaly and Peters anomaly.[ncbi.nlm.nih.gov] syndrome (ARS) belong to the overlapping spectrum of disorders summarized as anterior segment dysgenesis (ASD).[ncbi.nlm.nih.gov] Abstract Mutations within the RIEG1 homeobox gene on chromosome 4q25 have previously been reported in association with Rieger syndrome.[ncbi.nlm.nih.gov]

    Missing: coucher
  • Cat Eye Syndrome

    Abstract We describe a case of cat eye syndrome with 47,XX, 22q--. A balanced translocation, 46,XX,t(11;22), was found by banding studies in the mother. The clinical and cytogenetic correlations disclosed by a review of sporadic and familial cases illustrate the heterogeneity of the syndrome and the challenge to[…][ncbi.nlm.nih.gov]

    Missing: coucher

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