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Skull malformation such that the forehead is triangular
trigonon 'triangle' and kephale 'head'. Trigonocephaly can either occur in a syndrome or isolated, all by itself. Trigonocephaly is associated with the following
Trigonocephaly
Variant in human skulls
defects. Both metopic ridge and trigonocephaly involve premature fusion of the metopic suture. Like with trigonocephaly, there is no single proven cause
Metopic_ridge
X-linked recessive disorder characterised by developmental delay
classified the disorder as trigonocephaly with minor anomalies. They considered it different from trigonocephaly because trigonocephaly only deals with a deformed
Say–Meyer_syndrome
Surgical treatment
Netherlands; therefore, it is the most common form of craniosynostosis. In trigonocephaly, the metopic suture is prematurely fused. The metopic suture is situated
Craniofacial_surgery
Medical condition
Fryns–Aftimos syndrome (also known as Baraitser–Winter syndrome 1, or BWS1) is a rare chromosomal condition and is associated with pachygyria, severe intellectual
Fryns–Aftimos_syndrome
Premature fusion of bones in the skull
craniosynostosis. The condition is four times more common in boys than in girls. Trigonocephaly is a result from the premature closure of the metopic suture. According
Craniosynostosis
Trigger finger Trigonocephaly Trigonocephaly bifid nose acral anomalies Trigonocephaly broad thumbs Trigonocephaly ptosis coloboma Trigonocephaly ptosis mental
List_of_diseases_(T)
Medical condition
Trigonocephaly-bifid nose-acral anomalies syndrome is a very rare genetic disorder which is characterized by trigonobrachycephaly, narrow forehead, up-ward
Trigonocephaly-bifid nose-acral anomalies syndrome
Trigonocephaly-bifid_nose-acral_anomalies_syndrome
Medical condition
Curry–Jones syndrome is a rare genetic disorder characterized by congenital brain, osseous, cutaneous, ocular, and intestinal anomalies. Individuals with
Curry–Jones_syndrome
Human genetic disorder
Chitayat–Hall syndrome Person showing facial features of SYS, such as: Trigonocephaly and tooth malposition. Also limb contractures can be seen. Specialty
Schaaf–Yang_syndrome
Genetic disorder of the skull and face
abnormal head shape. This is present in combinations of: frontal bossing, trigonocephaly (fusion of the metopic suture), brachycephaly (fusion of the coronal
Crouzon_syndrome
Congenital disorder of the skull and digits
leads to different patterns of growth on the skull. Examples include: trigonocephaly (fusion of the metopic suture), brachycephaly (fusion of the coronal
Apert_syndrome
Medical condition
kyphoscoliosis, precocious puberty, obesity and the facial signs are: trigonocephaly, depressed nasal bridge, broad nose, small jaw, high-arched palate.
Temple_syndrome
Presence of abundant hair between the eyebrows
Siderius type Syndromic X-linked intellectual disability Snyder type Trigonocephaly 1 Uruguay Faciocardiomusculoskeletal syndrome Waardenburg syndrome types
Unibrow
Midline joint of the forehead
(craniosynostosis), it will cause a keel-shaped deformity of the skull called trigonocephaly. Its presence in a fetal skull, along with other cranial sutures and
Frontal_suture
List of medical conditions involving craniosynostosis
Retrieved 2023-07-06. "Trigonocephaly 1 (Concept Id: C0432122)". www.ncbi.nlm.nih.gov. Retrieved 2023-07-03. "Trigonocephaly 2 (Concept Id: C3280974)"
List of conditions with craniosynostosis
List_of_conditions_with_craniosynostosis
Medical condition
bartleby.com. Boston Children's Hospital 2013. "Metopic Synostosis (Trigonocephaly) - Boston Children's Hospital". childrenshospital.org.{{cite web}}:
Metopism
Medical condition
distinctive facial features like: Small head (microcephaly) Pointed forehead (trigonocephaly) Small ears which are low-set Widely-spaced eyes (hypertelorism) Droopy
Jacobsen_syndrome
Skull malformation such that the head is long and narrow
syndrome TCF12-related craniosynostosis Teebi hypertelorism syndrome 1 Trigonocephaly-short stature-developmental delay syndrome TWIST1-related craniosynostosis
Scaphocephaly
Group of congenital brain or skull defects
(Q75.0) Oxycephaly (Q75.0) Plagiocephaly (Q67.3) Scaphocephaly (Q75.0) Trigonocephaly (Q75.0) Polycephaly (Q89.4) Cyclopia Encephalocele MOMO syndrome Positional
Cephalic_disorder
Genetic disease resulting in abnormal formation or function of cilia
SUFU Branchio‐oculo‐facial syndrome 113620 TFAP2A C syndrome (Opitz trigonocephaly) 211750 CD96 Carpenter syndrome 201000 RAB23 Cephaloskeletal dysplasia
Ciliopathy
Fusion of two or more bones
[circular reference] Craniosynostosis has following kinds: scaphocephaly, trigonocephaly, plagiocephaly, anterior plagiocephaly, posterior plagiocephaly, brachycephaly
Synostosis
Medical condition
to refer to microcephaly. List of conditions with craniosynostosis Trigonocephaly (isolated metopic synostosis) Vinchon, Matthieu; Pellerin, Philippe;
Leptocephaly
Surname list
Smith–Lemli–Opitz syndrome, a metabolic and developmental disorder Opitz trigonocephaly syndrome, type of cephalic disorder Opitz–Kaveggia syndrome, genetic
Opitz
Medical condition
less common types of McGillivray syndromes are: Metopic synostosis (trigonocephaly). The metopic suture runs from the baby's nose to the sagittal suture
McGillivray_syndrome
orofacial anomalies Polysyndactyly overgrowth syndrome Polysyndactyly trigonocephaly agenesis of corpus callosum Polysyndactyly type 4 Polysyndactyly type
List_of_diseases_(P)
Medical condition
2 Brazilian brothers with growth delays, intellectual disabilities, trigonocephaly, microcephaly, preauricular tags, and cleft palate. They did a follow-up
Mandibulofacial dysostosis-microcephaly syndrome
Mandibulofacial_dysostosis-microcephaly_syndrome
Protein found in humans
Antley-Bixler syndrome (isoleucine-to-threonine at amino acid 300 (I300T), and trigonocephaly (mutation the same as the one for the Antley-Bixler syndrome viz., I300T)
Fibroblast growth factor receptor 1
Fibroblast_growth_factor_receptor_1
Medical condition
synostosis, oxycephaly, prominent metopic ridge, sagittal craniosynostosis, trigonocephaly, turricephaly Nervous system: Chiari malformation, seizures, syringomelia
Craniosynostosis and dental anomalies
Craniosynostosis_and_dental_anomalies
also been associated Jackson–Weiss syndrome, Antley-Bixler syndrome, Trigonocephaly, osteoglophonic dysplasia, squamous cell lung cancer and autosomal dominant
List of human clusters of differentiation
List_of_human_clusters_of_differentiation
Protein found in humans
member of the immunoglobulin superfamily, cause a form of the C (Opitz trigonocephaly) syndrome". American Journal of Human Genetics. 81 (4): 835–841. doi:10
CD96
deficiency; 609015; HADHA Trifunctional protein deficiency; 609015; HADHB Trigonocephaly; 190440; FGFR1 Trimethylaminuria; 602079; FMO3 Triphalangeal thumb,
List_of_OMIM_disorder_codes
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