About: McGillivray syndrome

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McGillivray syndrome is a rare syndrome characterized mainly by heart defects, skull and facial abnormalities and ambiguous genitalia. The symptoms of this syndrome are ventricular septal defect, patent ductus arteriosus, small jaw, undescended testes, and webbed fingers. Beside to these symptoms there are more symptoms which is related with bone structure and misshape.

Attributes	Values
rdf:type	Thing Disease yago:WikicatCongenitalDisordersOfEye,Ear,FaceAndNeck yago:WikicatCongenitalDisordersOfGenitalOrgans yago:Abnormality114501726 yago:Abstraction100002137 yago:Anomaly114505821 yago:Attribute100024264 yago:BirthDefect114465048 yago:Condition113920835 yago:Defect114464005 yago:Imperfection114462666 yago:PhysicalCondition114034177 disease yago:State100024720
rdfs:label	متلازمة مكجيليفري (ar) McGillivray syndrome (en)
rdfs:comment	متلازمة مَكجيليفري هي متلازمة نادرة تتميز بشكل أساسي بعيوب قلبية، وتشوّهات في الجمجمة والوجه، وأعضاء تناسلية ملتبسة. تشمل أعراض متلازمة مَكجيليفري عيب الحاجز البطيني، وبقاء القناة الشريانية مفتوحة، وصغر حجم الفك، وخصيتان غير نازلتان، وأصابع وتراء. إلى جانب الأعراض آنفة الذكر، قد يطوّر المرضى مزيدًا من الأعراض التي تتعلق ببنية العظام وتشكّلها. (ar) McGillivray syndrome is a rare syndrome characterized mainly by heart defects, skull and facial abnormalities and ambiguous genitalia. The symptoms of this syndrome are ventricular septal defect, patent ductus arteriosus, small jaw, undescended testes, and webbed fingers. Beside to these symptoms there are more symptoms which is related with bone structure and misshape. (en)
foaf:name	McGillivray syndrome (en)
name	McGillivray syndrome (en)
foaf:depiction
dcterms:subject	Congenital disorders of genital organs Syndromes with craniofacial abnormalities Rare syndromes Congenital heart defects Congenital disorders of eye, ear, face and neck
Wikipage page ID	36442937 (xsd:integer)
Wikipage revision ID	1052868438 (xsd:integer)
Link from a Wikipage to another Wikipage	Hereditary Craniectomy Coronal synostosis Congenital disorders of genital organs Virchow Syndromes with craniofacial abnormalities Odilon Lannelongue Sagittal suture Endoscopy Brachycephaly Brain Coronal suture Anesthesia Patent ductus arteriosus Joint Lambdoid suture Fontanel Ambiguous genitalia Rare syndromes Congenital heart defects Birth defect Trigonocephaly Congenital disorders of eye, ear, face and neck Metopic suture Microcephaly Cephalometry Scalp Skull Ventricular septal defect Imbecile Scaphocephaly Endoscopic surgery Heart defect Cranial suture Computerized Tomography Undescended testes Ossified dbr:Calvarial dbr:Craniosynostectomy dbr:Lambdoid_synostosis dbr:Strip_craniectomy
Link from a Wikipage to an external page	https://docs.google.com/document/d/1Z4L2UUyAlfR6_E9pCgdWjdv0Y0kp8GeOJpRASUmn46Y/edit%23 https://www.ncbi.nlm.nih.gov/sites/ga%3Fdisorder=McGillivray%20syndrome http://rarediseases.info.nih.gov/GARD/Disease.aspx%3FPageID=4&diseaseID=3426
sameAs	McGillivray syndrome McGillivray syndrome McGillivray syndrome McGillivray syndrome McGillivray syndrome
dbp:wikiPageUsesTemplate	dbt:Cn dbt:Empty_section dbt:Infobox_medical_condition_(new) dbt:Medical_resources dbt:Male_congenital_malformations_of_genital_organs,_indeterminate_sex_and_pseudohermaphroditism dbt:Female_congenital_malformations_of_genital_organs
thumbnail	wiki-commons:Special:FilePath/Autosomal_dominant_-_en.svg?width=300
ICD	Q87.0 (en)
OMIM	609579 (xsd:integer)
Orphanet	168624 (xsd:integer)
caption	This condition is inherited via an autosomal dominant manner (en)
field	cardiology (en)
synonyms	Familial scaphocephaly syndrome, McGillivray type, Scaphocephaly-macrocephaly-maxillary retrusion-intellectual disability syndrome (en)
has abstract	متلازمة مَكجيليفري هي متلازمة نادرة تتميز بشكل أساسي بعيوب قلبية، وتشوّهات في الجمجمة والوجه، وأعضاء تناسلية ملتبسة. تشمل أعراض متلازمة مَكجيليفري عيب الحاجز البطيني، وبقاء القناة الشريانية مفتوحة، وصغر حجم الفك، وخصيتان غير نازلتان، وأصابع وتراء. إلى جانب الأعراض آنفة الذكر، قد يطوّر المرضى مزيدًا من الأعراض التي تتعلق ببنية العظام وتشكّلها. متلازمة ماكغليفراي هي عيب ولادي، يلحتم مفصل واحد أو أكثر بين عظام جمجمة الطفل قبل الأوان، أي قبل أن يتطوّر دماغ الطفل بالشكل الكامل. عندما يعاني الطفل من تعظم الدروز الباكر، لا يستطيع دماغه أن ينمو في شكله الطبيعي ويبدو الرأس مشوهًا. يمكن أن يؤثر هذا العيب على واحد أو أكثر من المفاصل في جمجمة الطفل. عادةً ما ينطوي علاج مَكجيليفري على جراحة لفصل العظام الملتحمة. في حال عدم وجود خلل في الدماغ، تتيح الجراحة لدماغ الطفل بالنمو والتطور ضمن حيّز كافي. (ar) McGillivray syndrome is a rare syndrome characterized mainly by heart defects, skull and facial abnormalities and ambiguous genitalia. The symptoms of this syndrome are ventricular septal defect, patent ductus arteriosus, small jaw, undescended testes, and webbed fingers. Beside to these symptoms there are more symptoms which is related with bone structure and misshape. McGillivray syndrome is a birth defect in which one or more of the joints between the bones of the baby's skull close prematurely, before the baby's brain is fully formed. When the baby has craniosynostosis, his or her brain cannot grow in its natural shape and the head is misshapen. It can affect one or more of the joints in the baby's skull. In some cases, craniosynostosis is associated with an underlying brain abnormality that prevents the brain from growing properly. Treating McGillivray usually involves surgery to separate the fused bones. If there is no underlying brain abnormality, the surgery allows the baby's brain to grow and develop in adequate space. (en)
gold:hypernym	Syndrome
prov:wasDerivedFrom	wikipedia-en:McGillivray_syndrome?oldid=1052868438&ns=0
page length (characters) of wiki page	10574 (xsd:nonNegativeInteger)
ICD10	Q87.0
OMIM id	609579 (xsd:integer)
ORPHA	168624
foaf:isPrimaryTopicOf	wikipedia-en:McGillivray_syndrome

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