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140 Possible Causes for Sagittal Suture Craniosynostosis

  • Craniosynostosis

    Sagittal craniosynostosis is the most common type of non-syndromic craniosynostosis and occurs when the sagittal suture fuses before birth.[gosh.nhs.uk] […] over the sagittal suture.[uclahealth.org] Generally, symptoms of craniosynostosis syndromes are specific to the suture involved and time of diagnosis.[eyewiki.aao.org]

  • Familial Scaphocephaly Syndrome

    Generally, symptoms of craniosynostosis syndromes are specific to the suture involved and time of diagnosis.[eyewiki.aao.org] Isolated occurrence with unknown etiology is common, mostly affecting the sagittal suture.[ommbid.mhmedical.com] Sagittal Craniosynostosis (Scaphocephaly) Sagittal craniosynostosis is the most common form of craniosynostosis, occurring in about 1 in 2000 live births.[craniofacial.vcu.edu]

  • Craniosytosis Type 4

    Generally, symptoms of craniosynostosis syndromes are specific to the suture involved and time of diagnosis.[eyewiki.aao.org] Types of single suture craniosynostosis: Sagittal synostosis fusion of the midline sagittal suture; growth fails to occur across the head and excessive growth occurs from[headlines.org.uk] Isolated occurrence with unknown etiology is common, mostly affecting the sagittal suture.[ommbid.mhmedical.com]

  • Isolated Synostotic Plagiocephaly

    What is Pediatric Sagittal Synostosis? Sagittal craniosynostosis (scaphocephaly) is the most common form of isolated craniosynostosis.[childrens.com] Generally, symptoms of craniosynostosis syndromes are specific to the suture involved and time of diagnosis.[eyewiki.aao.org] The most common forms of non-syndromic craniosynostosis affect the sagittal (most common), coronal, metopic and lambdoidal sutures.[chop.edu]

  • Isolated Trigonocephaly

    Generally, symptoms of craniosynostosis syndromes are specific to the suture involved and time of diagnosis.[eyewiki.aao.org] Isolated occurrence with unknown etiology is common, mostly affecting the sagittal suture.[ommbid.mhmedical.com] The most common forms of non-syndromic craniosynostosis affect the sagittal (most common), coronal, metopic and lambdoidal sutures.[chop.edu]

  • Cloverleaf Skull

    Generally, symptoms of craniosynostosis syndromes are specific to the suture involved and time of diagnosis.[eyewiki.aao.org] Scaphocephaly Lateral Radiograph - Scaphocephaly CT 3D reconstruction - posterior sagittal suture fusion Plagiocephaly Plagiocephaly - Craniosynostosis.[paeds.co.uk] […] in the sagittal plane, and a triangular appearance in the axial plane A form of craniosynostosis where multiple sutures of the skull prematurely fuse, causing the skull to[quizlet.com]

  • Acrocephalopolysyndactyly

    sagittal craniosynostosis lambdoid sutures craniosynostosis pilonidal dimple absent coccyx spina bifida occulta scoliosis coxa v alga decreased hip-joint mobility flared[humpath.com] (fusion of the metopic and sagittal sutures) (2) facial deformity (3) polysyndactyly of the toes and brachyclinosyndactyly of the fingers (4) obesity (5) cardiac malformations[meducator3.net] In many affected infants and children, craniosynostosis initially involves the sutures between bones forming the upper sides and the back of the skull (i.e., sagittal and[rarediseases.org]

  • Craniosynostosis-Dandy-Walker Malformation-Hydrocephalus Syndrome

    These causes include hydrocephalus (congenital/acquired), subdural effusions (SDEs), sagittal suture craniosynostosis, Dandy–Walker malformation (DWM), tumors, and arachnoid[thieme-connect.com] Classification of craniosynostosis Non-syndromic Suture involved Simple Scaphocephaly Sagittal Anterior plagiocephaly Unilateral coronal Posterior plagiocephaly Unilateral[thefreelibrary.com] Saethre-Chotzen, Jackson-Weiss, Carpenter’s, cloverleaf skull Sagittal synostosis This is the most common type of craniosynostosis.[cmej.org.za]

  • Psychomotor Retardation

    This deletion involves 18 genes; FGF2, NUDT6, and SPRY1 are primarily or secondarily implicated in human cranial bone and sagittal suture development and could play an important[ncbi.nlm.nih.gov] CASE REPORT: We describe an unusual clinical case with an 11-Mb deletion at 4q27 (chr4: 123094652-134164491), craniosynostosis (CS), mild psychomotor retardation, and facial[ncbi.nlm.nih.gov]

  • Marfan Syndrome

    Shprintzen-Goldberg syndrome (SGS) is characterized by: craniosynostosis of the coronal, sagittal, or lambdoid sutures; dolichocephaly; distinctive craniofacial features;[ncbi.nlm.nih.gov] […] usually involving the coronal, sagittal, or lambdoid sutures Craniofacial findings Dolichocephaly with or without scaphocephaly Tall or prominent forehead Ocular proptosis[ncbi.nlm.nih.gov] Diagnosis Clinical Diagnosis The diagnosis of Shprintzen-Goldberg syndrome (SGS) is suspected in individuals with a combination of the following major characteristics: Craniosynostosis[ncbi.nlm.nih.gov]

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