Turkish: Causes & Reasons

Possible Causes for Turkish

Thus, the regional origin should be regarded as a determining factor in the diagnosis of FMF in Turkish patients. [ncbi.nlm.nih.gov]

Tunca M, Akar S, Onen F, Ozdogan H, Kasapcopur O, Yalcinkaya F, Tutar E, Ozen S, Topaloglu R, Yilmaz E, Arici M, Bakkaloglu A, Besbas N, Akpolat T, Dinc A, Erken E, Turkish [doi.org]

844TC genotype may be protective in the studied Turkish population. [ncbi.nlm.nih.gov]

Behçet Disease

Clinical Utility The HLA class I molecule HLA-B51 is the most strongly associated risk factor and has been shown to be associated with Behçet’s in Turkish and Asian patients [kashilab.com]

Email: alismjawad1@hotmail.com In 1937, Professor Hulusi Behçet, a Turkish dermatologist, described two cases of relapsing ulceration of the mouth, eye and genitalia, a triple [web.archive.org]

National Team 10.11 102 Nazim Bakirci - Turkish National Team 103 Nico Graf - Atlas-Romer's Hausbäckerei 11.32 104 Dominique Cornu - Silence-Lotto 12.24 105 Francis De Greef [feltet.dk]

Amyloidosis in Familial Mediterranean Fever

[…] reported the distribution of the mutations in the carrier chromosomes of FMF-amyloidosis patients. 2–4 We have now completed the analysis of MEFV mutation analysis in 44 Turkish [pediatrics.aappublications.org]

The mortality rate among Turkish patients was high, but this high rate may have represented selection bias. [emedicine.medscape.com]

Evaluating MEFV mutation frequency in Turkish familial Mediterranean fever suspected patients and gender correlation: a retrospective study. [ijbms.mums.ac.ir]

Acro-Pectoral Syndrome

Here we report a six generation Turkish family with a related but distinct dominantly inherited acropectoral syndrome. [go.gale.com]

It has been described in 22 patients from a six-generation Turkish family. It is transmitted as an autosomal dominant trait and the causative gene is located at 7q36. [monarchinitiative.org]

Here we report a large six generation Turkish family (fig 1) with a related but distinct combination of distal limb and sternal abnormalities, also inherited in an autosomal [go.gale.com]

Dursun Syndrome

Brasil Two Turkish siblings with MEGDEL syndrome due to novel SERAC1 gene mutation. [pesquisa.bvs.br]

@article{nal2015TwoTS, title={Two Turkish siblings with MEGDEL syndrome due to novel SERAC1 gene mutation.}, author={{\"O}zlem Serpil {\"U}nal and Rıza K{\"o}ksal {\"O}zg{ [semanticscholar.org]

The affected infants were of Turkish descent and developed respiratory distress on their second day of life. [symptoma.com]

Scimitar Syndrome

Case 1 In P-A lung graph, Scimitar (Turkish Sword) finding. [oatext.com]

Scimitar syndrome is named for the crescent- or Turkish sword-like shadow in the chest radiography and is often associated with hypoplasia of the right lung and right pulmonary [mesh.kib.ki.se]

(Figure 1) Case 2 Figure 1: Scimitar (Turkish sword) finding in the P-A lung graph. [oatext.com]

Cenani Syndactylism

(July 2017) Eponym[edit] The syndrome is named after Turkish (Asim Cenani) and German (Widukind Lenz) medical geneticists.[7][8] References[edit] ^ a b Temtamy SA, Ismail [en.wikipedia.org]

The syndrome was named after two medical geneticists; Turkish geneticist Asim Cenani, and German geneticist Widukind Lenz. [dianamossop.com]

You can help by adding to it. ( July 2017 ) Eponym The syndrome is named after Turkish ( Asim Cenani ) and German ( Widukind Lenz ) medical geneticists. [7] [8] References [popflock.com]

Congenital Scoliosis due to Bony Malformation

By sequencing the entire protein-coding regions of the genome of a young Turkish girl with the disease and two of her affected family members, the scientists found that an [riken.jp]

We conducted a study on a Turkish family with an AR brachyolmia, with the aim of identifying a disease gene for AR brachyolmia. [keio.pure.elsevier.com]

All three had forms of brachyolmia that clinically mirrored those found in the Turkish family, and all three had loss-of-function mutations in both copies of their PAPSS2 [riken.jp]

Neuronal Ceroid Lipofuscinosis Type 8

[…] juvenile (Batten-Spielmeyer-Vogt disease) CLN6 NCL 6/Neuronal ceroid lipofuscinosis, late infantile (Kufs type) CLN8 NCL 8/ laat infantiele Neuronale Ceroid Lipofuscinose (Turkish [lumc.nl]

There are two forms of this mutated gene: 1-CLN8 and 2-CLN8. 1-CLN8 is known as Northern epilepsy syndrome, while 2-CLN8 is primarily from Turkish descent. [en.wikipedia.org]

Mole and Anna‐Elina Lehesjoki, Variant late infantile neuronal ceroid lipofuscinosis in a subset of Turkish patients is allelic to Northern epilepsy, Human Mutation, 23, 4 [doi.org]

Pulmonary Alveolar Microlithiasis

Ucan ES, Keyt AI, Aydilek R, Yalcin Z, Sehit S, Kudu M, Ok U (1993) Pulmonary alveolar microlithiasis: review of Turkish reports. [doi.org]

A 12-year-old girl of Turkish descent was referred 6 weeks after an influenza A infection because of persistent chest X-ray abnormalities compatible with interstitial lung [ncbi.nlm.nih.gov]

Abstract Two asymptomatic Turkish sibs are presented, a 4-year-old boy and his 7-year-old sister, with pulmonary alveolar microlithiasis (PAM) confirmed by transbronchial [doi.org]

Analbuminemia

Pregledni rad https://doi.org/10.11613/BM.2016.031 A nucleotide deletion and frame-shift cause analbuminemia in a Turkish family. [hrcak.srce.hr]

The analbuminemic trait was diagnosed in a young Turkish woman on the basis of her clinical symptoms (bilateral lower limb edema) and biochemical findings (minimal albumin [ncbi.nlm.nih.gov]

[…] continuing study of the molecular genetics of congenital analbuminemia, we report here the clinical and biochemical findings and the mutation analysis of the gene in two Turkish [hrcak.srce.hr]

Warburg Micro Syndrome 3

[…] doi: 10.1097/MCD.0b013e328054c404 ORIGINAL ARTICLES Abstract Author Information Authors Article Metrics Metrics We report a 4-year-old Turkish boy with Warburg Micro syndrome [journals.lww.com]

Medicine, Biology Human Genetics 2010 A novel homozygous RAB3GAP2 small in-frame deletion is reported that causes Warburg Micro syndrome in a girl from a consanguineous Turkish [semanticscholar.org]

Case presentation: We describe four siblings from healthy consanguineous Turkish parents with developmental delay, congenital cataract, and speech delay. [tandfonline.com]

Mulibrey Nanism Syndrome

"A novel splice site mutation in the TRIM37 gene causes mulibrey nanism in a Turkish family with phenotypic heterogeneity". Hum. [ipfs.io]

"A novel mutation in TRIM37 is associated with mulibrey nanism in a Turkish boy". Clinical Dysmorphology 16 (3): 173–176. doi : 10.1097/MCD.0b013e3280f6d00b. [wiki30.com]

"A novel mutation in TRIM37 is associated with mulibrey nanism in a Turkish boy". Clinical Dysmorphology. 16 (3): 173–176. doi : 10.1097/MCD.0b013e3280f6d00b. [ipfs.io]

Infantile Neuronal Ceroid Lipofuscinosis

Am J Hum Genet 2002 Variant late infantile neuronal ceroid lipofuscinosis in a subset of Turkish patients is allelic to Northern epilepsy Ranta et al. [pubfacts.com]

More recently, it has been found that a subset of a Turkish variant of late infantile NCL (v-LINCL) is also associated with CLN8 mutations. [springerlink.com]

Late Infantile NCL variants were the Finnish variant, the Indian-Costa-Rican-Portuguese variant, and the Turkish variant. [ncl-netz.de]

Mesoaxial Synostotic Syndactyly with Phalangeal Reduction

We identified another published report of this phenotype in a large, inbred Turkish family. [ncbi.nlm.nih.gov]

MethodsFifty-four patients with MDD who received citalopram and 70 controls from the Turkish population were genotyped for ABCB1 C3435T polymorphism. [scipers.com]

First linkage was reported to chromosome 2q31 in a large Turkish family (Sarfarazi et al. 1995). [en.youscribe.com]

Cold-Induced Sweating Syndrome Type 1

The aim of this study was to report on three new patients with CS and review the Turkish patients. [ingentaconnect.com]

[…] impairment, and cognitive delay. 24 Al-Sayed MD...Kaya N 24075186 2013 8 Multiple small hyperintense lesions in the subcortical white matter on cranial MR images in two Turkish [malacards.org]

A and B, Pedigrees of the five Sardinian and three Turkish families. [pubmed.ncbi.nlm.nih.gov]

Neuronal Ceroid Lipofuscinosis Type 7

Acronym CLN7 Synonyms Turkish variant late infantile NCL Keywords Any medical or genetic information present in this entry is provided for research, educational and informational [uniprot.org]

CLN7 The CLN7 gene has been assigned to the Turkish LINCL (tLINCL) variant. Individuals with the tLINCL variant were thought to originate from Turkey. [emedicine.medscape.com]

[…] juvenile (Batten-Spielmeyer-Vogt disease) CLN6 NCL 6/Neuronal ceroid lipofuscinosis, late infantile (Kufs type) CLN8 NCL 8/ laat infantiele Neuronale Ceroid Lipofuscinose (Turkish [lumc.nl]

Ulnar Mammary Syndrome

Abstract We present a large Turkish family with autosomal dominant inherited ulnar-mammary syndrome in which 10 affected family members, spanning three generations, were diagnosed [ncbi.nlm.nih.gov]

Pediatri Arşivi; Yıl: 1998 Cilt: 33 Sayı: 4 ISSN : 1306-0015 Language : tur Type : Journal Article In AGRIS since : 2016 Publisher : Galenos Yayınevi All titles : " The First Turkish [agris.fao.org]

PubMedCentral PubMed CrossRef Google Scholar Wollnik B, Kayserili H, Uyguner O, Tukel T, Yuksel-Apak M (2002) Haploinsufficiency of TBX3 causes ulnar-mammary syndrome in a large Turkish [link.springer.com]

Hepatoportal Sclerosis

The aim of the study was to summarize the clinical features of Turkish patients with HPS and to measure the serum levels of interleukin (IL)-6 and interferon (IFN)-gamma to [ncbi.nlm.nih.gov]

We conclude that genetic predisposition might be a possible factor for HPS development in Turkish patients and it should be kept in mind that cholestatic features noticed [ncbi.nlm.nih.gov]

[…] sclerosis as a cause of noncirrhotic portal hypertension in patients with HIV. ( 17640321 ) 2007 37 Clinical features, serum interleukin-6, and interferon-gamma levels of 34 turkish [malacards.org]

Neuronal Ceroid Lipofuscinosis Type 10

CLN7 The CLN7 gene has been assigned to the Turkish LINCL (tLINCL) variant. Individuals with the tLINCL variant were thought to originate from Turkey. [emedicine.medscape.com]

Variant late infantile neuronal ceroid lipofuscinosis in a subset of Turkish patients is allelic to Northern epilepsy. Hum Mutat. 2004;23:300–5. [ncbi.nlm.nih.gov]

Siintola et al identified 6 mutations in 5 families, 4 Turkish families and 1 Indian family, in the MFSD8 gene. The authors mapped the locus to 4q28.1-q28.2. [emedicine.medscape.com]

Acrocallosal Syndrome

A 6 month old Turkish boy with the acrocallosal syndrome is reported. [ncbi.nlm.nih.gov]

Five Turkish patients including dizygotic twins are reported. [ncbi.nlm.nih.gov]

Five Turkish patients including dizygotic twins are reported. a Department of Medical Genetics, GATA Medical School, Ankara, Turkey b Department of Medical Genetics Adnan [journals.lww.com]

Aerodontalgia

Hebrew Hindi Hungarian Icelandic Indonesian Italian Japanese Korean Lao Norwegian Polish Portuguese Romanian Russian Slovak Slovenian Spanish Swahili Swedish Tamil Thai Turkish [definition.org]

עברית (Hebrew) Gaeilge (Irish) Українська (Ukrainian) اردو (Urdu) Magyar (Hungarian) मानक हिन्दी (Hindi) Indonesia (Indonesian) Italiano (Italian) தமிழ் (Tamil) Türkçe (Turkish [definitions.net]

Eunuchism

Total number of language pairs : 472 Total number of translations : 14 New : Korean Turkish, Serbian Albanian, Dutch German, Latvian Russian Improved : English Albanian, English [eudict.com]

[…] about improving this site Interface translation : Tomislav Kuzmić ( Croatian ), Vasudevan Tirumurti, Fahim Razick ( Tamil ), Matti Tapanainen ( Finnish ), Ebru Bağlan ( Turkish [eudict.com]

Transient Hypogammaglobulinemia of Infancy

In this study, we analysed the B cell subsets of patients with an initial THI diagnosis (n = 20) and compared them with those of healthy age-matched Turkish children (n = [ncbi.nlm.nih.gov]

[…] clinical features FMF TRAPS HIDS FCAS MWS NOMID/CINCA usual ethnicity Turkish, Armenian, Arab, Jewish, Italian any ethnicity Dutch, other Northern European mostly European [ufrgs.br]

[…] transiently elevated in the early childhood of transient hypogammaglobulinemia of infancy patients. ( 21531630 ) Rutkowska M....Siedlar M. 2011 13 New laboratory findings in Turkish [malacards.org]

Limb-Girdle Muscular Dystrophy Type 2G

Next generation sequencing analysis detected a homozygous frameshift mutation in the TCAP gene (c.90_91del), previously described in one Turkish family. [helda.helsinki.fi]

In a group of 38 autosomal recessive Turkish LGMD families Dincer et al. (2000) detected 7 CAPN3, 3 DYSF, 2 SGCA, 7 SGCB, 5 SGCG, 1 SGCD and 2 LAMA2 deficiencies. [dmd.nl]

LGMD2K This extremely rare form of LGMD has been reported in Turkish individuals. Onset is during infancy or early childhood. [rarediseases.org]

Congenital Neuronal Ceroid Lipofuscinosis

CLN7 The CLN7 gene has been assigned to the Turkish LINCL (tLINCL) variant. Individuals with the tLINCL variant were thought to originate from Turkey. [emedicine.medscape.com]

Variant late infantile neuronal ceroid lipofuscinosis in a subset of Turkish patients is allelic to Northern epilepsy. Hum Mutat. 2004;23:300–5. [ncbi.nlm.nih.gov]

Siintola et al identified 6 mutations in 5 families, 4 Turkish families and 1 Indian family, in the MFSD8 gene. The authors mapped the locus to 4q28.1-q28.2. [emedicine.medscape.com]

Congenital Generalized Lipodystrophy Type 4

We report our clinical experience on two unrelated Turkish patients with congenital generalized lipodystrophy type 4. [ncbi.nlm.nih.gov]

PTRF mutations and detailed phenotypes of two male and three female patients with CGL4 belonging to two pedigrees of Mexican origin (CGL7100 and CGL178) and one pedigree of Turkish [ncbi.nlm.nih.gov]

Title: Spectrum of clinical manifestations in two young Turkish patients with congenital generalized lipodystrophy type 4. [ncbi.nlm.nih.gov]

Muscular Dystrophy-Dystroglycanopathy Type C9

In a group of 38 autosomal recessive Turkish LGMD families Dincer et al. (2000) detected 7 CAPN3, 3 DYSF, 2 SGCA, 7 SGCB, 5 SGCG, 1 SGCD and 2 LAMA2 deficiencies. [dmd.nl]

LGMD2K This extremely rare form of LGMD has been reported in Turkish individuals. Onset is during infancy or early childhood. [rarediseases.org]

A few cases have been described in Turkish and English families. LGMD 2L (fukutin) Childhood There is deterioration of weakness with viral infections. [patient.info]

Parametritis

History Play ENTRENus Play ENTRENuk Play ENTRENau Meanings of "parametritis" in Turkish English Dictionary : 2 result(s) Category English Turkish Medical 1 Medical parametritis [tureng.com]

History Meanings of "parametritis and pelvic cellulitis" in Turkish English Dictionary : 1 result(s) Category English Turkish Pathology 1 Pathology parametritis and pelvic [tureng.com]

[…] paraüretrit 2 Medical parametritis parametrit Meanings of "parametritis" with other terms in English Turkish Dictionary : 3 result(s) Category English Turkish Pathology 1 [tureng.com]

Late-Infantile Neuronal Ceroid Lipofuscinosis

CLN7 The CLN7 gene has been assigned to the Turkish LINCL (tLINCL) variant. Individuals with the tLINCL variant were thought to originate from Turkey. [emedicine.medscape.com]

[…] juvenile (Batten-Spielmeyer-Vogt disease) CLN6 NCL 6/Neuronal ceroid lipofuscinosis, late infantile (Kufs type) CLN8 NCL 8/ laat infantiele Neuronale Ceroid Lipofuscinose (Turkish [lumc.nl]

Batten disease/NCL group: •Finnish Late Infantile – identified in Finland •Variant Late Infantile – identified in Costa Rica, South America, Portugal and other nations •Turkish [bradysbattle.wordpress.com]