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Longer titles found: Craniosynostosis, Adelaide type (view), Craniosynostosis, Philadelphia type (view), Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome (view), Craniosynostosis-fibular aplasia syndrome (view), Craniosynostosis and dental anomalies (view), Craniosynostosis with anomalies of the cranial base and digits (view), Craniosynostosis–anal anomalies–porokeratosis syndrome (view), List of conditions with craniosynostosis (view)

searching for Craniosynostosis 46 found (190 total)

alternate case: craniosynostosis

Boomerang dysplasia (824 words) [view diff] no match in snippet view article find links to article

Boomerang dysplasia is a lethal form of osteochondrodysplasia known for a characteristic congenital feature in which bones of the arms and legs are malformed

Carpenter syndrome (1,676 words) [view diff] exact match in snippet view article find links to article

the skull. The two most common types of craniosynostosis are sagittal and bicoronal. Sagittal craniosynostosis manifests itself by causing a long narrow

Osteogenesis imperfecta (15,363 words) [view diff] no match in snippet view article find links to article

Osteogenesis imperfecta (IPA: /ˌɒstioʊˈdʒɛnəsɪs ˌɪmpɜːrˈfɛktə/; OI), colloquially known as brittle bone disease, is a group of genetic disorders that all

McGillivray syndrome (1,341 words) [view diff] exact match in snippet view article find links to article

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

Gómez–López-Hernández syndrome (1,614 words) [view diff] exact match in snippet view article find links to article

1016/s0387-7604(79)80039-x. PMID 95427. S2CID 4698879. López-Hernández, A (2013). "Craniosynostosis, ataxia, trigeminal anaesthesia and parietal alopecia with pons-vermis

Cardiocranial syndrome, Pfeiffer type (186 words) [view diff] exact match in snippet view article find links to article

disorder syndrome characterized by congenital heart defects, sagittal craniosynostosis, and severe developmental delay. The condition has been reported in

Zoltan Vajo (1,737 words) [view diff] exact match in snippet view article find links to article

and acanthosis nigricans), Thanatophoric dysplasia, Muenke coronal craniosynostosis and Crouzon syndrome as well as more recently on genetically engineered

List of diseases (S) (1,934 words) [view diff] exact match in snippet view article

type Short rib-polydactyly syndrome, Verma-Naumoff type Short ribs craniosynostosis polysyndactyly Short stature abnormal skin pigmentation mental retardation

Molera (821 words) [view diff] exact match in snippet view article find links to article

premature closure of the skull base cranial sutures (brachycephaly due to craniosynostosis). To accommodate the developing brain there is increased growth of

List of diseases (H) (1,717 words) [view diff] exact match in snippet view article

Herpetophobia Herrmann–Opitz arthrogryposis syndrome Herrmann–Opitz craniosynostosis Hers' disease Hersh–Podruch–Weisskopk syndrome Heterophobia Heterotaxia

Adducted thumb syndrome (396 words) [view diff] exact match in snippet view article find links to article

and talipes equinovarus or calcaneovalgus. It is characterized by craniosynostosis, and myopathy in association with congenital generalized hypertrichosis

Karin Muraszko (1,466 words) [view diff] exact match in snippet view article find links to article

Buchman, Steven R. (March 2016). "Endoscopic Strip Craniectomy for Craniosynostosis". Journal of Craniofacial Surgery. 27 (2): 293–298. doi:10.1097/SCS

Thanatophoric dysplasia (852 words) [view diff] exact match in snippet view article find links to article

disorders: the achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricans". Endocr. Rev. 21 (1):

Severe achondroplasia with developmental delay and acanthosis nigricans (849 words) [view diff] exact match in snippet view article find links to article

Mutation Confirmation, Pre-symptomatic, Risk Assessment, Screening Craniosynostosis: Diagnosis Invitae FGFR3-Related Disorders Test: Pre-symptomatic, Diagnosis

List of diseases (M) (2,469 words) [view diff] exact match in snippet view article

Marfan-like syndrome, Boileau type Marfan-like syndrome Marfanoid craniosynostosis syndrome Marfanoid hypermobility Marfanoid mental retardation syndrome

Fibroblast growth factor receptor (827 words) [view diff] exact match in snippet view article find links to article

14109. PMC 5362545. PMID 28030802. GeneReviews/NIH/NCBI/UW entry on FGFR-Related Craniosynostosis Syndromes FGF signaling (with refs) Portal: Biology

List of diseases (L) (900 words) [view diff] exact match in snippet view article

dysplasia dwarfism Larsen-like syndrome lethal type Larsen syndrome craniosynostosis Larsen syndrome, dominant type Larsen syndrome, recessive type Larsen

Sensenbrenner syndrome (897 words) [view diff] exact match in snippet view article find links to article

acromesomelic shortening, craniofacial characteristics with absence of craniosynostosis, small kidneys with tubular and glomerular microscopic cysts, persistent

List of diseases (B) (1,032 words) [view diff] exact match in snippet view article

dysplasia lethal Holmgren type Bone dysplasia Moore type Bone fragility craniosynostosis proptosis hydrocephalus Bone marrow failure neurologic abnormalities

Homo heidelbergensis (8,374 words) [view diff] exact match in snippet view article find links to article

adolescent SH skull (Cranium 14) was diagnosed with lambdoid single suture craniosynostosis (immature closing of the left lambdoid suture, leading to skull deformities

Multisystem developmental disorder (860 words) [view diff] exact match in snippet view article find links to article

PMID 17907517. Kamath, BM; Stolle, C; Bason, L; Colliton, RP; et al. (2002). "Craniosynostosis in Alagille syndrome". American Journal of Medical Genetics. 112 (2):

Chromosome 15 (3,031 words) [view diff] exact match in snippet view article find links to article

the long arm of chromosome 15: confirmation of a causative role in craniosynostosis and definition of a 15q25-qter trisomy syndrome". Am J Med Genet. 87

Fibroblast growth factor 8 (2,175 words) [view diff] exact match in snippet view article find links to article

sequence, and mapping of human FGF8 with no evidence for its role in craniosynostosis/limb defect syndromes". American Journal of Medical Genetics. 72 (3):

John A. Jane (398 words) [view diff] exact match in snippet view article find links to article

David Yashon) (1969) Scientific foundations and surgical treatment of craniosynostosis (with John A. Persing and Milton T. Edgerton) (1989) Craniofacial surgery :

Interleukin 11 (2,522 words) [view diff] exact match in snippet view article find links to article

L (October 2018). "IL11RA-related Crouzon-like autosomal recessive craniosynostosis in 10 new patients: Resemblances and differences". Clinical Genetics

ACSL3 (1,075 words) [view diff] exact match in snippet view article find links to article

Herwerden L, Chotai KA, Winter RM (Oct 1992). "The mapping of a gene for craniosynostosis: evidence for linkage of the Saethre-Chotzen syndrome to distal chromosome

Derek Steinbacher (719 words) [view diff] exact match in snippet view article find links to article

facial differences like cleft lip and palate, skull abnormalities (craniosynostosis), small or disproportioned jaws, and TMJ ankyloses (fusions). Steinbacher

Achondroplasia (4,575 words) [view diff] exact match in snippet view article find links to article

Disorders: The Achondroplasia Family of Skeletal Dysplasias, Muenke Craniosynostosis, and Crouzon Syndrome with Acanthosis Nigricans". Endocrine Reviews

SNAI1 (1,850 words) [view diff] exact match in snippet view article find links to article

human snail (SNAI1) gene and exclusion as a major disease gene in craniosynostosis". Human Genetics. 105 (4): 320–6. doi:10.1007/s004390051108. PMID 10543399

Cytochrome P450 reductase (2,454 words) [view diff] exact match in snippet view article find links to article

in 2004. The index patient was a newborn 46,XX Japanese girl with craniosynostosis, hypertelorism, mid-face hypoplasia, radiohumeral synostosis, arachnodactyly

Susan Durham (161 words) [view diff] exact match in snippet view article find links to article

Dartmouth Institute for Health Policy and Clinical Science. Durhams treats craniosynostosis, peripheral nerve and brachial plexus lesions, spina bifida, pediatric

Plastic surgery (6,316 words) [view diff] exact match in snippet view article find links to article

skeleton and soft tissues, such as cleft lip and palate, microtia, craniosynostosis, and pediatric fractures. Adult craniofacial surgery deals mostly with

List of human clusters of differentiation (467 words) [view diff] exact match in snippet view article find links to article

numerous medical conditions including abnormal bone development (e.g. craniosynostosis syndromes) and cancer. Five Prime has a monoclonal antibody, FPA144

Le Fort osteotomy (367 words) [view diff] exact match in snippet view article find links to article

I distraction osteogenesis using an internal device for syndromic craniosynostosis". Journal of Oral and Maxillofacial Surgery. 72 (4): 788–95. doi:10

Neural tube defect (5,814 words) [view diff] exact match in snippet view article find links to article

ISSN 2472-1727. PMC 6511489. PMID 30421543. CDC (2019-12-04). "Facts about Craniosynostosis | CDC". Centers for Disease Control and Prevention. Retrieved 2022-11-28

Clair Francomano (828 words) [view diff] exact match in snippet view article find links to article

Disorders: The Achondroplasia Family of Skeletal Dysplasias, Muenke Craniosynostosis, and Crouzon Syndrome with Acanthosis Nigricans*". Endocrine Reviews

Ali Rıza Öreroğlu (1,038 words) [view diff] exact match in snippet view article find links to article

Surg. 2013;21(2):10-15. Concurrent repair of orbital shallowness with craniosynostosis surgery: two late cases of simultaneous orbital decompression. Öreroğlu

List of human evolution fossils (7,280 words) [view diff] exact match in snippet view article find links to article

Miguel-Ángel (2010-06-01). "The earliest evidence of true lambdoid craniosynostosis: the case of "Benjamina", a Homo heidelbergensis child". Child's Nervous

Munis Dundar (869 words) [view diff] exact match in snippet view article find links to article

neurological development, short height, pylorus stenosis, pectus excavatum, craniosynostosis, large ears, thin upper lip and bilateral cryptorchidism were reported

Avizo (software) (6,118 words) [view diff] exact match in snippet view article

Huang, C.S. (2012). "Fronto-facial monobloc distraction in syndromic craniosynostosis. Three-dimensional evaluation of treatment outcome and facial growth"

Alain Goriely (2,718 words) [view diff] exact match in snippet view article find links to article

level, he proposed the first mechanical models of craniectomy and craniosynostosis through systematic mathematical modeling, analysis and computational

Salé cranium (1,194 words) [view diff] exact match in snippet view article find links to article

Miguel-Ángel (2010-06-01). "The earliest evidence of true lambdoid craniosynostosis: the case of "Benjamina", a Homo heidelbergensis child". Child's Nervous

Peter J. Taub (1,423 words) [view diff] exact match in snippet view article find links to article

association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9. Nat Genet. 2012 Dec;44(12):1360-4. doi:

PRP36 (2,052 words) [view diff] exact match in snippet view article find links to article

Nassogne MC, Wyns E, Sibille C (Nov 2009). "A new case of syndromic craniosynostosis with cryptic 19p13.2-p13.13 deletion". American Journal of Medical

Developmental bioelectricity (17,264 words) [view diff] exact match in snippet view article find links to article

Miyatake, S.; Hayashidani, M.; et al. (2014). "Aortic aneurysm and craniosynostosis in a family with Cantu syndrome". American Journal of Medical Genetics

List of OMIM disorder codes (18,877 words) [view diff] exact match in snippet view article find links to article

123000; ANKH Cranioosteoarthropathy; 259100; HPGD Craniosynostosis, type 1; 123100; TWIST1 Craniosynostosis, type 2; 604757; MSX2 CRASH syndrome; 303350;