Craniosynostosis affects the majority of mucopolysaccharidosis patients and can contribute to increased intracranial pressure

scientific article published on 06 August 2018

Craniosynostosis affects the majority of mucopolysaccharidosis patients and can contribute to increased intracranial pressure is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1007/S10545-018-0212-1
P932PMC publication ID6326980
P698PubMed publication ID30083803

P50authorMirjam LangeveldQ55948686
Ans van der PloegQ88008512
Esmee OussorenQ88499253
George J G RuijterQ130279286
P2093author name stringIrene M J Mathijssen
Jan C van der Meijden
Margreet Wagenmakers
Rob M Verdijk
Hansje H Bredero-Boelhouwer
Marie-Lise C van Veelen-Vincent
Johanna M P van den Hout
P2860cites workEvidence-Based Medicine: Nonsyndromic CraniosynostosisQ48222386
Mucopolysaccharidosis type I with craniosynostosis.Q50575918
Brain and spine MRI features of Hunter disease: frequency, natural evolution and response to therapy.Q51873956
A population-based study of craniosynostosis in metropolitan Atlanta, 1989-2003.Q51961876
Tracing craniosynostosis to its developmental stage through bone center displacement.Q52175646
Mucopolysaccharidosis type I and craniosynostosis.Q53099264
Craniosynostosis in Western Australia, 1980-1994: a population-based studyQ56379512
A population-based study of craniosynostosisQ56396444
Optic nerve head swelling and optic atrophy in the systemic mucopolysaccharidosesQ68369003
New insights into craniofacial malformationsQ28088384
The timing of physiologic closure of the metopic suture: a review of 159 patients using reconstructed 3D CT scans of the craniofacial regionQ28205803
Guideline for Care of Patients With the Diagnoses of Craniosynostosis: Working Group on CraniosynostosisQ28607705
Virchow and the pathogenesis of craniosynostosis: a translation of his original workQ30459823
Report of a mucopolysaccharidosis occurring in Australian aboriginesQ33588412
Disc oedema in association with Hunter's syndrome: ocular histopathological findingsQ33643474
Slit ventricle syndrome and early-onset secondary craniosynostosis in an infantQ33769372
Mucopolysaccharidosis VI.Q33863356
Single-suture craniosynostosis: a review of neurobehavioral research and theoryQ34359996
Overcoming the barriers to diagnosis of Morquio A syndromeQ34789123
Long-term functional outcome in 167 patients with syndromic craniosynostosis; defining a syndrome-specific risk profileQ35012869
Sinus pericranii involving the torcular sinus in a patient with Hunter's syndrome and trigonocephaly: case report and review of the literatureQ35864916
Hydrocephalus and mucopolysaccharidoses: what do we know and what do we not know?Q36395552
Long-term cognitive follow-up in children treated for Maroteaux-Lamy syndromeQ36582221
Normocephalic pancraniosynostosis resulting in late presentation of elevated intracranial pressuresQ37741736
Altered FGF signalling in congenital craniofacial and skeletal disordersQ38674265
Craniosynostosis update 1987.Q39607907
Sutural biology and the correlates of craniosynostosisQ40793420
The incidence of isolated craniosynostosis in the newborn infant.Q44958828
Mutation screening in patients with syndromic craniosynostoses indicates that a limited number of recurrent FGFR2 mutations accounts for severe forms of Pfeiffer syndromeQ46898196
Developmental and behavioral aspects of mucopolysaccharidoses with brain manifestations - Neurological signs and symptoms.Q47668549
Surgical management of neurological manifestations of mucopolysaccharidosis disordersQ47962754
P433issue6
P921main subjectcraniosynostosisQ378183
P304page(s)1247-1258
P577publication date2018-08-06
P1433published inJournal of Inherited Metabolic DiseaseQ6295359
P1476titleCraniosynostosis affects the majority of mucopolysaccharidosis patients and can contribute to increased intracranial pressure
P478volume41

Reverse relations

Q89503466Posterior fossa horns; a new calvarial finding of mucopolysaccharidoses with well-known cranial MRI featurescites workP2860

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