About: Neu–Laxova syndrome

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Neu–Laxova syndrome (NLS, also known as Neu syndrome; Neu-Povysilová syndrome; or 3-phosphoglycerate dehydrogenase deficiency, neonate form) is a rare autosomal recessive disorder characterized by severe intrauterine growth restriction and multiple congenital malformations. Neu–Laxova syndrome is a very severe disorder, leading to stillbirth or death shortly after birth. It was first described by Dr. Richard Neu in 1971 and Dr. Renata Laxova in 1972 as a lethal disorder in siblings with multiple malformations. Neu–Laxova syndrome is an extremely rare disorder with less than 100 cases reported in medical literature.

Attributes	Values
rdf:type	Thing Disease disease
rdfs:label	متلازمة نيو-لاكسوفا (ar) Neu-Laxova-Syndrom (de) Neu–Laxova syndrome (en) Zespół Neua-Laxovy (pl)
rdfs:comment	متلازمة نيو-لاكسوفا (المعروفة أيضًا باسم متلازمة نيو اختصارا) هي اضطراب وراثي متنحي نادر الحدوث (أقل من 100 حالة في الأدبيات الطبية)، يتميز بوجود تقييد مفرط لنمو الجنين داخل الرحم، ووجود عيوب خلقية متعددة. وصف المتلازمة لأول مرة كل من الطبيب ريتشارد نيو (عام 1971) والطبيبة ريناتا لاكسوفا (عام 1972) على أنها اضطراب مُميت يصاحبة تشوهات متعددة، وتُعتبر متلازمة نيو-لاكسوفا أحد الاضطرابات الشديدة التي تؤدي إلى ولادة جنين ميت أو تتسبب في وفاته بعد الولادة بوقت قصير. (ar) Das Neu-Laxová-Syndrom (auch: Neu-Syndrom, Neu-Povysilová-Syndrom; abgekürzt NLS; engl. Neu-Laxová syndrome) ist ein absolut letal verlaufendes angeborenes Fehlbildungssyndrom, gekennzeichnet durch ein behindertes Wachstum des Fötus und eine Reihe körperlicher Missbildungen. (de) Neu–Laxova syndrome (NLS, also known as Neu syndrome; Neu-Povysilová syndrome; or 3-phosphoglycerate dehydrogenase deficiency, neonate form) is a rare autosomal recessive disorder characterized by severe intrauterine growth restriction and multiple congenital malformations. Neu–Laxova syndrome is a very severe disorder, leading to stillbirth or death shortly after birth. It was first described by Dr. Richard Neu in 1971 and Dr. Renata Laxova in 1972 as a lethal disorder in siblings with multiple malformations. Neu–Laxova syndrome is an extremely rare disorder with less than 100 cases reported in medical literature. (en) Zespół Neua-Laxovy (zespół Neua-Povysilovy, ang. Neu-Laxová syndrome, Neu's syndrome, Neu-Povysilová syndrome, NLS) – letalny zespół wewnątrzmacicznego zahamowania wzrostu i mnogich malformacji. (pl)
dcterms:subject	Syndromes with cleft lip and/or palate Syndromes with craniofacial abnormalities Autosomal recessive disorders Syndromes with dysmelia Congenital disorders Rare syndromes Syndromes affecting the nervous system Disorders related to length of gestation and fetal growth
Wikipage page ID	44611130 (xsd:integer)
Wikipage revision ID	1121073050 (xsd:integer)
Link from a Wikipage to another Wikipage	Homozygous Hyperkeratosis Renata Laxova Intrauterine growth restriction PSPH Syndromes with cleft lip and/or palate Syndromes with craniofacial abnormalities Cleft lip Cleft palate Glycine Autosomal recessive disorders Lissencephaly Stillbirth Compound heterozygosity Ichthyosis Autosomal recessive Agenesis of the corpus callosum Syndromes with dysmelia Edema Cell growth Central nervous system Proptosis Congenital disorders Rare syndromes Syndromes affecting the nervous system Syndactyly Disorders related to length of gestation and fetal growth Metabolic disorder Microcephaly Micrognathia Neural tube defect Cerebellar hypoplasia Serine Congenital abnormality Polyhydramnios PSAT1 Microgyria PHGDH 3-phosphoglycerate dehydrogenase deficiency Genetic counselling
sameAs	Neu–Laxova syndrome Neu–Laxova syndrome Neu–Laxova syndrome Neu–Laxova syndrome Neu–Laxova syndrome Neu–Laxova syndrome Neu–Laxova syndrome
dbp:wikiPageUsesTemplate	dbt:Citation_needed dbt:Medical_resources dbt:Refimprove dbt:Reflist dbt:Infobox_medical_condition dbt:OMIM
ICD	759.890000 (xsd:double) (en) Q87.8 (en)
OMIM	256520 (xsd:integer)
synonym	Neu-Povysilová syndrome; Neu syndrome; 3-phosphoglycerate dehydrogenase deficiency, neonate form (en)
has abstract	متلازمة نيو-لاكسوفا (المعروفة أيضًا باسم متلازمة نيو اختصارا) هي اضطراب وراثي متنحي نادر الحدوث (أقل من 100 حالة في الأدبيات الطبية)، يتميز بوجود تقييد مفرط لنمو الجنين داخل الرحم، ووجود عيوب خلقية متعددة. وصف المتلازمة لأول مرة كل من الطبيب ريتشارد نيو (عام 1971) والطبيبة ريناتا لاكسوفا (عام 1972) على أنها اضطراب مُميت يصاحبة تشوهات متعددة، وتُعتبر متلازمة نيو-لاكسوفا أحد الاضطرابات الشديدة التي تؤدي إلى ولادة جنين ميت أو تتسبب في وفاته بعد الولادة بوقت قصير. (ar) Das Neu-Laxová-Syndrom (auch: Neu-Syndrom, Neu-Povysilová-Syndrom; abgekürzt NLS; engl. Neu-Laxová syndrome) ist ein absolut letal verlaufendes angeborenes Fehlbildungssyndrom, gekennzeichnet durch ein behindertes Wachstum des Fötus und eine Reihe körperlicher Missbildungen. (de) Neu–Laxova syndrome (NLS, also known as Neu syndrome; Neu-Povysilová syndrome; or 3-phosphoglycerate dehydrogenase deficiency, neonate form) is a rare autosomal recessive disorder characterized by severe intrauterine growth restriction and multiple congenital malformations. Neu–Laxova syndrome is a very severe disorder, leading to stillbirth or death shortly after birth. It was first described by Dr. Richard Neu in 1971 and Dr. Renata Laxova in 1972 as a lethal disorder in siblings with multiple malformations. Neu–Laxova syndrome is an extremely rare disorder with less than 100 cases reported in medical literature. (en) Zespół Neua-Laxovy (zespół Neua-Povysilovy, ang. Neu-Laxová syndrome, Neu's syndrome, Neu-Povysilová syndrome, NLS) – letalny zespół wewnątrzmacicznego zahamowania wzrostu i mnogich malformacji. (pl)
ICD9	759.89
prov:wasDerivedFrom	wikipedia-en:Neu–Laxova_syndrome?oldid=1121073050&ns=0
page length (characters) of wiki page	8181 (xsd:nonNegativeInteger)
ICD10	Q87.8
OMIM id	256520 (xsd:integer)
foaf:isPrimaryTopicOf	wikipedia-en:Neu–Laxova_syndrome
is Link from a Wikipage to another Wikipage of	D-glycerate dehydrogenase deficiency Dysmelia PSPH Phosphoglycerate dehydrogenase Ichthyosis Acrocallosal syndrome Ciliopathy Neu-Laxova syndrome List of syndromes Morse–Rawnsley–Sargent syndrome PSAT1

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