Turkish: Causes & Reasons

Possible Causes for Turkish

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

History Meanings of "familial mediterranean fever" in Turkish English Dictionary : 1 result(s) Category English Turkish Medical 1 Medical familial mediterranean fever ailevi [tureng.com]

Based on these observations, the ACE I/D variant D/D genotypes implicate a possible risk in the FMF-related amyloidosis among Turkish population. [ncbi.nlm.nih.gov]

Behçet Disease

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]

Researchers conducted a genome-wide association study (GWAS) that enrolled 1,209 Turkish people affected by Behcet's disease and 1,278 unaffected Turkish people - all residents [disabled-world.com]

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]

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

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

Etymology It was first described by Asim Cenani, a Turkish medical geneticist and Widukind Lenz, a German medical geneticist in 1967 2. [radiopaedia.org]

Abstract We describe an additional case of Cenani-Lenz syndactylism in a 4 1/2-year-old boy from a consanguineous Turkish family. [unboundmedicine.com]

VL - 70 IS - 4 N2 - We describe an additional case of Cenani-Lenz syndactylism in a 4 1/2-year-old boy from a consanguineous Turkish family. [unboundmedicine.com]

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]

METHODS: We studied four apparently unrelated patients who had congenital analbuminemia: two of Amerindian and two of Turkish origin. [ncbi.nlm.nih.gov]

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]

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]

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]

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]

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]

However, a majority of cases reported so far were of Turkish origin. [orpha.net]

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]

Acro-Pectoral Syndrome

Here we report a six generation Turkish family with a related but distinct dominantly inherited acropectoral syndrome. [avesis.erciyes.edu.tr]

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]

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]

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]

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]

Our aim was to emphasize the familial character and the clinical features of the disease, and to draw attention to the increasing number of Turkish patients reported in the [ncbi.nlm.nih.gov]

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 lung biopsy [ncbi.nlm.nih.gov]

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]

Aerodontalgia

English Arabic German English Spanish French Hebrew Italian Japanese Dutch Polish Portuguese Romanian Russian Swedish Turkish Ukrainian Chinese French Synonyms Arabic German [context.reverso.net]

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

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]

Ulnar Mammary Syndrome

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]

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]

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]

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]

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]

[…] 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]

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]

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]

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 new Turkish infant with clinical features of CS/CISS1 syndrome and homozygous CRLF1 mutation. Eur J Med Genet 2014;57:212-5. 27. [jcnonweb.com]

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]

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]

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]

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]

Geographic Tongue

OBJECTIVE: The aim of this study was to investigate the frequency of benign migratory glossitis (BMG) in a Turkish population with respect to gender, age, smoking, atopic [ncbi.nlm.nih.gov]

The prevalence and risk factors associated with benign migratory glossitis lesions in 7619 Turkish dental outpatients. [ncbi.nlm.nih.gov]

The prevalence and risk fasctors associated with benign migratory glossitis lesions in. 7619 Turkish dental outpatients. [wydawnictwo.ump.edu.pl]

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]

Transmembrane Late infantile (Turkish) ? CLN7 Transporter protein Transmembrane, lysosomal Late infantile (northern epilepsy mental retardation) (TLC protein class) ? [medlink.com]

Splenitis

[…] splenectomia splenetico splenico splenio splenite splenomegalia splenotomia splitting spocchia spocchioso spodestare spodosol spoetizzare spogliare spogliarellista In the Turkish-English [en.bab.la]

[…] translations in other languages: Chinese (zh) Czech (cs) Finnish (fi) French (fr) Italian (it) Kurdish Kurmanji (ku) Malay (ms) Persian (fa) Slovenian (sl) Spanish (es) Thai (th) Turkish [glosbe.com]

[…] splenitis 80 millions of speakers Translator Malay - Tamil splenitis 75 millions of speakers Translator Malay - Marathi प्लीहादाह 75 millions of speakers Translator Malay - Turkish [educalingo.com]