Dutch: Causes & Reasons

Possible Causes for Dutch

Heterozygous Familial Hypercholesterolemia

Table 2 The Dutch Diagnostic Criteria. [ncbi.nlm.nih.gov]

HeFH can be diagnosed using DNA testing or by utilizing one of three well-accepted sets of criteria — Simon Broome (UK), Dutch Lipid Clinic Network (Netherlands), or MEDPED [patientworthy.com]

FH is more common among certain ethnic or racial groups, such as those of French Canadian, Finnish, Lebanese, and Dutch descent. [healthline.com]

Familial Hypercholesterolemia Type 1

Prevalence rates were assessed using the Dutch Lipid Clinics Network (DLCN) and the US-MEDPED criteria. We stratified for gender and age. [ncbi.nlm.nih.gov]

Potential FH was estimated using Dutch Lipid Clinic Network (DLCN) criteria. Potential FH was defined as having a total score≥6. [ncbi.nlm.nih.gov]

The FH phenotype was classified according to the Dutch Lipid Clinic Network criteria. [ncbi.nlm.nih.gov]

Late-Onset Pompe Disease

Clinical manifestation and natural course of late-onset Pompe's disease in 54 Dutch patients. Brain 2005;128:671–677 [PubMed] [Google Scholar] 3. [ncbi.nlm.nih.gov]

Clinical manifestation and natural course of late-onset Pompe’s disease in 54 Dutch patients. Brain 2005; 128: 671-7. 25. Desnuelle C, Salviati L. [medicinabuenosaires.com]

Clinical manifestation and natural course of lateonset Pompe’s disease in 54 Dutch patients. Brain. 2005;128:671–677. [ncbi.nlm.nih.gov]

Hereditary Hyperekplexia

A survey of various symptoms of hyperekplexia was performed in the Dutch pedigree. Linkage studies were performed for these symptoms. [ncbi.nlm.nih.gov]

Design: A survey of various symptoms of hyperekplexia was performed in the Dutch pedigree. Linkage studies were performed for these symptoms. [doi.org]

The patients are part of the Dutch hyperekplexia pedigree. [ncbi.nlm.nih.gov]

Chondritis of the External Ear

DutchICPC2-ICD10ENG Thesaurus Dutch MTHU059685 L3688232no S4371467 Y pinna; perichondritis Dutch(ICD10DUT) ICD10, Dutch Translation H61.0 L3717675no S4400910 Y Perichondritis [doctor.am]

Perichondritis and chondritis of pinna Italian Pericondrite dell'orecchio, Pericondrite del padiglione auricolare, non specificata, Pericondrite del padiglione auricolare Dutch [fpnotebook.com]

Thesaurus Dutch MTHU055600 L3684728no S4367963 Y oorschelp; perichondritis DutchICPC2-ICD10ENG Thesaurus Dutch MTHU058699 L3687377no S4370613 Y perichondritis; oor DutchICPC2 [doctor.am]

Folliculotropic Mycosis Fungoides

Type and results of initial treatment were retrieved from the Dutch Registry. [ncbi.nlm.nih.gov]

Recommendations for treatment in folliculotropic mycosis fungoides: Report of the Dutch Cutaneous Lymphoma Group. [rug.nl]

[…] and May 2014 at a tertiary referral center hosting the Dutch Cutaneous Lymphoma Registry. [ncbi.nlm.nih.gov]

Hyper-IgD Syndrome

Also known as: Hyperimmunoglobulinemia D and Periodic Fever Syndrome Periodic Fever Dutch Type. [autoinflammatory.uk]

Wikidata Jump to navigation Jump to search No description defined HIDS Hyperimmunoglobulinemia D and Periodic Fever Syndrome Hyperimmunoglobulinemia D syndrome Periodic Fever, Dutch [wikidata.org]

Hyper-IgD syndrome clusters in children of Dutch, French, and other Northern European ancestry and is caused by Mutations in the gene coding mevalonate kinase, an enzyme important [merckmanuals.com]

Familial Hypercholesterolemia

[…] sensitivity, specificity, positive and negative predictive values for the LDL-C quartile distribution, LDL-C as a continuous variable, as well as the performance measures for the Dutch [ncbi.nlm.nih.gov]

Objective: To compare the validity of the Dutch Lipid Clinic Network (DLCN), Simon Broome (SB), Make Early Diagnosis to Prevent Early Deaths (MEDPED), and American Heart Association [ncbi.nlm.nih.gov]

According to the Dutch Lipid Clinic Network criteria, 18.4% of the patients had definite FH, 66.0% had probable FH, and 15.6% had possible FH. [ncbi.nlm.nih.gov]

Variegate Porphyria

Africa by Dutch settlers at the end of the 17th century. [ncbi.nlm.nih.gov]

Families carrying these mutations test negative for the R59W mutation, and are not related to the large family descended from the original Dutch settlers. [porphyria-professionals.uct.ac.za]

[…] original descriptions are attributed to Hippocrates, the disease was first explained biochemically by Felix Hoppe-Seyler in 1871, and acute porphyrias were described by the Dutch [indigitrax.org.au]

Adult Krabbe Disease

English, French, German, Italian, Norwegian, Portuguese, Spanish), text or web page Babylon translation program, free (English to Spanish, German, Portuguese, French, Italian, Dutch [kumc.edu]

[…] disease ペルテス病 GeorgClemens Perthes （1869-1927） German surgeon Peutz-Jegher ポイツ・ジェガース Peutz-Jeghers syndrome ポイツ・ジェガース症候群 JohannesLaurentius Augustinus Peutz （1886-1957） Dutch [jams.med.or.jp]

It has been described to account for 44% of the alleles of American patients with Northern European ancestry and for 52% of unrelated Dutch cases. [ncbi.nlm.nih.gov]

Congenital Cyst of Canal of Nuck

Arabic Bulgarian Chinese Croatian Czech Danish Dutch English Estonian Finnish French German Greek Hebrew Hindi Hungarian Icelandic Indonesian Italian Japanese Korean Latvian [dictionary.sensagent.com]

History and etymology Persistence of the processus vaginalis peritonei (i.e. the canal of Nuck) was first described by Anton Nuck (Dutch anatomist, 1650-1692) in 1691 2. [radiopaedia.org]

Malagasy Norwegian Persian Polish Portuguese Romanian Russian Serbian Slovak Slovenian Spanish Swedish Thai Turkish Vietnamese Arabic Bulgarian Chinese Croatian Czech Danish Dutch [dictionary.sensagent.com]

Spinocerebellar Ataxia Type 19

Abstract The SCA19 locus on chromosome 1p21-q21 was identified in a Dutch family in 2002. [ncbi.nlm.nih.gov]

Scientific Papers 129 Downloads 18 Citations Abstract The SCA19 locus on chromosome 1p21-q21 was identified in a Dutch family in 2002. [link.springer.com]

References Identification of a novel SCA locus ( SCA19) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21. [wikigenes.org]

Properdin Deficiency

We have identified the genetic defect in 10 Dutch families. Six different mutations and one sequence polymorphism in the properdin gene were found. [doi.org]

To better understand the dysfunctional protein on the molecular level, samples from three members of the Dutch family were analyzed by direct genomic sequencing. [ncbi.nlm.nih.gov]

[…] properdin is characterized by complete absence (type I), very low level presence (type II), or the presence of a dysfunctional properdin protein in serum as found in one Dutch [ncbi.nlm.nih.gov]

Autosomal Recessive Spastic Paraplegia Type 7

PMID: 22964162 [PubMed – in process] Genotype-phenotype correlations in spastic paraplegia type 7: a study in a large Dutch cohort. van Gassen KL, van der Heijden CD, de Bot [hspersunite.org.au]

Genotype-phenotype correlations in spastic paraplegia type 7: a study in a large Dutch cohort. Brain. 2012 Sep 10. [Epub ahead of print]. [disorders.eyes.arizona.edu]

[…] paraplegia type 55 Early-onset autosomal dominant Alzheimer disease Hereditary cerebral hemorrhage with amyloidosis, Arctic type Hereditary cerebral hemorrhage with amyloidosis, Dutch [csbg.cnb.csic.es]

Pitted Keratolysis

Dutch physicians prefer combined topical antibiotic therapy with non-pharmacological treatments and perceive the efficacy of topical antibiotic therapy superior to non-pharmacological [ncbi.nlm.nih.gov]

MedDRA Dutch 10069447 L9059697 preferred S11301395 N pitted keratolysis Dutch MedDRA Dutch 10069447 L9059697 preferred S11301395 Y pitted keratolysis English (RCD) Read Codes [doctor.am]

Suykerbuyk, Pitted keratolysis; physicians’ treatment and their perceptions in Dutch army personnel, Journal of the European Academy of Dermatology and Venereology, 2013, [onlinelibrary.wiley.com]

Klein-Waardenburg Syndrome

[…] a meeting of the Dutch Ophthalmological Society ( Waardenburg 1948 ). [medlink.com]

[…] a meeting of the Dutch Ophthalmological Society (Waardenburg 1948). [medlink.com]

DURING recent years a number of reports 1-7 have shown that Waardenburg's syndrome, once believed to occur only in Dutch people, does occur in many ethnic groups. [jamanetwork.com]

Autosomal Recessive Spastic Paraplegia Type 27

Our study of 18 Dutch SPG11-patients shows the potential serious long-term consequences of SPG11 including a possibly restricted life span. [nature.com]

Juvenile amyotrophic lateral sclerosis-dementia complex in a Dutch family. Neurology. 1968;18:800-06. 33. Hentati A, Ouahchi K, Pericak-Vance MA, et al. [demneuropsy.com.br]

[…] frontotemporal dementia, 27,28 but only the ï¬rst type is allegedly associated with mental retarda- tion in JALS reports. 29,30 A JALS/dementia cluster has also been described in Dutch [redalyc.org]

Bullous Dystrophy Type Macular

Two families (one of whom was Dutch and the other Italian) have been described up to now, in which only males were affected. Transmission is X-linked recessive. [malacards.org]

This disorder had been observed in only a single Dutch kindred ({4:Hassing and Doeglas, 1980}) until a second family with bullous dystrophy was described by {5:Lungarotti [bio2rdf.org]

Fine mapping places the bullous dystrophy locus distal to DXS102 (Xq26.3) in the Italian family and distal to DXS998 (Xq27.3) in the Dutch family. [ncbi.nlm.nih.gov]

Spinocerebellar Ataxia Type 23

= "We have recently identified missense mutations in prodynorphin (PDYN), the precursor to dynorphin opioid peptides, as the cause for spinocerebellar ataxia (SCA23) in Dutch [rug.nl]

We have identified missense mutations in prodynorphin (PDYN) that cause SCA23 in four Dutch families displaying progressive gait and limb ataxia. [ncbi.nlm.nih.gov]

Recently the prodynorphin (PDYN) gene was identified as the cause of SCA23 in four Dutch families displaying progressive gait and limb ataxia. [ncbi.nlm.nih.gov]

Pelger-Huet Anomaly

In 1931 Huet, a Dutch pediatrician, identified it as an inherited disorder. [askhematologist.com]

Pelger-Huët anomaly (pel″gĕr hū′ĕt) [Karel Pelger, Dutch physician, 1885–1931; Gauthier Jean Huët, Dutch physician, 1879–1970], PHA A benign autosomal dominant disorder of [medical-dictionary.thefreedictionary.com]

The characteristic leukocyte appearance was first reported in 1928 by Pelger, a Dutch hematologist, who described leukocytes with dumbbell-shaped bilobed nuclei, a reduced [askhematologist.com]

ADan Amyloidosis

\n\nThe Dutch type of hereditary cerebral amyloid angiopathy is the most common form. [ncbi.nlm.nih.gov]

The Dutch type of hereditary cerebral amyloid angiopathy is the most common form. [ncbi.nlm.nih.gov]

The Dutch type is the most common, with over 200 affected individuals reported in the scientific literature. [medlineplus.gov]

Van Buchem Disease

The Afrikaners have Dutch antecedants and it seems likely that these autosomal recessive disorders result from homozygosity of the same faulty genes. [ncbi.nlm.nih.gov]

In a group of Dutch patients the disease is thought to be due to a 52-kb deletion that results in decreased expression of the SOST gene. [ncbi.nlm.nih.gov]

Using an extended Dutch inbred van Buchem family and two inbred sclerosteosis families, we mapped both disease genes to the same region on chromosome 17q12-q21, supporting [ncbi.nlm.nih.gov]

Pompe Disease

Three mutations in the acid alpha-glucosidase gene are common in the Dutch patient population: IVS1(-13T-->G), 525delT and delexon18. 63% of Dutch GSD II patients carry one [ncbi.nlm.nih.gov]

Three mutations in the acid α-glucosidase gene are common in the Dutch patient population: IVS1(-13T→G), 525delT and delexon18 63% of Dutch GSD II patients carry one or two [doi.org]

Keywords: Alpha-galactosidase, cardiomyopathy, myopathy Introduction Pompe disease was first described in 1932 by the Dutch pathologist, JC Pompe, who observed glycogen storage [ncbi.nlm.nih.gov]

Mevalonate Kinase Deficiency

Abstract Dutch type periodic fever (DPF) is an autosomal recessive hereditary fever syndrome. [ncbi.nlm.nih.gov]

So for a Dutch patient marrying a Dutch partner, the chances of a child with HIDS are at most 1 in 1000. [hidsnet.wordpress.com]

It was first described in Dutch children in 1984 and is most common in North West Europe, especially in the Netherlands. [amyloidosis.org.uk]

Fetal Malnutrition

We investigated the effects of such well-studied polymorphisms and their interactions with fetal malnutrition on type 2 diabetes risk and related phenotypes in the Dutch Famine [ncbi.nlm.nih.gov]

Initial suggestions of long-term effects came from historical records: adults born to mothers who lived through famine conditions (such as the Dutch Hunger Winter of 1944/ [nestlenutrition-institute.org]

TABLE 1 General and maternal characteristics according to time of pregnancy when exposed to the Dutch famine All Born before Late gestation Mid-gestation Early gestation Conceived [diabetes.diabetesjournals.org]

Beriberi

The Dutch physician, Christaan Eijkman's classic experiments in the 1890s began to clarify the role of diet in the development of beriberi. [sharecare.com]

Adolphe Vorderman (1844-1902), a Dutch government doctor who worked in the Dutch East Indies, was one of the people who made careful observations on groups of humans receiving [jameslindlibrary.org]

At the end of the 19th century, Dutch physician Gerrit Grijns (1865-1944) from the University of Utrecht, working in Java in the Dutch East Indies (now Indonesia), developed [worldneurologyonline.com]

Hyperactive Airway Disease

DutchICPC2-ICD10ENG Thesaurus Dutch MTHU053770 L3683040no S4366274 Y obstructie; luchtweg, chronisch Dutch(ICD10DUT) ICD10, Dutch Translation J44.9 L3711317no S4394552 Y [doctor.am]

D and periodic fever syndrome; Periodic fever Dutch type; HIDS See More Categories: Hyper IgD syndrome is the less severe form of a metabolic disorder known as mevalonate [rarediseases.info.nih.gov]

ABri Amyloidosis

\n\nThe Dutch type of hereditary cerebral amyloid angiopathy is the most common form. [ncbi.nlm.nih.gov]

6011000124106~MAPRULE~IFA 703220002 | Hereditary cystatin C amyloid angiopathy | 6011000124106~MAPGROUP~2 6011000124106~MAPADVICE~IF HEREDITARY CEREBRAL AMYLOID ANGIOPATHY, DUTCH [bioportal.bioontology.org]

21: Aß peptide with precursor protein APP (chromosome 21): CAA related to familial Alzheimer disease CAA in Down syndrome hereditary cerebral hemorrhage with amyloidosis (Dutch [radiopaedia.org]

Peutz-Jeghers Syndrome

History and etymology The syndrome is named after Jans Peutz (1886-1957), a Dutch physician and Harold Jeghers (1904-1990), an American physician who had successively described [radiopaedia.org]

Peutz, Dutch physician, 1886-1957; Harold J. [medical-dictionary.thefreedictionary.com]

Peutz-Jeghers syndrome - see under Peutz Peutz, Johnnes Laurentius Augustinus, Dutch physician, 1886-1957. [medical-dictionary.thefreedictionary.com]

Familial Hyperlipidemia

Not all will qualify by the Dutch criteria.” Sniderman argues that the diagnosis of FH, instead of severe hypercholesterolemia, only confuses the issue. [cardiobrief.org]

Some populations, such as French Canadian and Dutch Afrikaner, have a prevalence as high as 1 in 100. Reference Interval See table. [beta.labcorp.com]

Using a modified version of the Dutch Lipid Clinic criteria, which classifies people with either definite or probable FH based on LDL cholesterol levels, physical examination [cardiobrief.org]