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Increased distance between the inner corners of the eyelids
telecanthus refers to telecanthus resulting from traumatic injury to the nasal-orbital-ethmoid (NOE) complex. The diagnosis of traumatic telecanthus requires
Telecanthus
Congenital anomaly in which the eye openings are small
the eyes also appear spaced more widely apart as a result, known as telecanthus. In addition to small palpebral fissures, features can include epicanthus
Blepharophimosis
Medical condition
Syndactyly, Telecanthus, and Anogenital and Renal malformations. The name STAR stands for the syndrome's primary signs and symptoms: Syndactyly Telecanthus Anogenital
STAR_syndrome
Genetic condition involving hearing loss and depigmentation
there is also a wider gap between the inner corners of the eyes called telecanthus, or dystopia canthorum. In type 3, which is rare, the arms and hands
Waardenburg_syndrome
Abnormally increased distance between two body parts, usually the eyes
pupils, is greater than normal. Hypertelorism should not be confused with telecanthus, in which the distance between the inner eye corners is increased, but
Hypertelorism
Genetic disorder caused by a mutation of chromosome 15
A five-year-old girl with Angelman syndrome. Features shown include telecanthus, bilateral epicanthic folds, small head, wide mouth, and an apparently
Angelman_syndrome
False appearance of crossed eyes
fully developed. The bridge of their nose is wide and flat, creating telecanthus (increased distance between medial canthus of both eyes). With age, the
Pseudostrabismus
Corner of the eye where the upper and lower eyelids meet
landmarks (single points representing the point of each commissural angle). Telecanthus, or dystopia canthorum, is a lateral displacement of the inner canthi
Canthus
Morphological phenomenon
consisting of features such as low-set ears, single transverse palmar crease, telecanthus, micrognathism, macrocephaly, hypotonia and furrowed tongue. While MPAs
Minor_physical_anomalies
Class of congenital medical conditions
including Möbius syndrome, broad nose, increased distance between the eyes (telecanthus), defects in the lower eyelids, and facial asymmetry. Limbs generally
Hanhart_syndrome
Telangiectasia, hereditary hemorrhagic Telangiectasia Telecanthus hypertelorism pes cavus Telecanthus with associated abnormalities Telencephalic leukoencephalopathy
List_of_diseases_(T)
Medical condition
hypotonia, intellectual disability and craniofacial anomalies including telecanthus and epicanthic fold. Also, thin corpus callosum or ventriculomegaly,
LINKED_syndrome
Medical condition
These include hypospadias-dysphagia syndrome, Opitz-Frias syndrome, telecanthus with associated abnormalities, and hypertelorism-hypospadias syndrome
Opitz_G/BBB_syndrome
Medical condition
blepharophimosis, in which palpebral aperture is reduced and there is telecanthus, but the eyelid margins are normal. Another condition similar to ankyloblepharon
Ankyloblepharon
Pinzer, T; Gollogly, J; Krishnan, KG; Schackert, G; Lauer, G (2008). "Telecanthus and hypertelorism in frontoethmoidal meningoencephaloceles and the surgical
Children's_Surgical_Centre
Medical condition
Holoprosencephaly Craniosynostosis Low-set ears Microphthalmia Hypertelorism Telecanthus Ptosis of the eyelid Down-slanting palpebral fissures Depression of the
Holoprosencephaly-ectrodactyly-cleft lip/palate syndrome
Holoprosencephaly-ectrodactyly-cleft_lip/palate_syndrome
Medical condition
not-so-common symptoms:[2] Oral frenulum abnormalities Bifid uvula Hypertelorism Telecanthus List of uncommon symptoms:[2] Missing/underdeveloped corpus callosum
Pai_syndrome
Medical condition
the disorder is its facial phenotype. Children have hypertelorism or telecanthus, small nose, short or sparse eyelashes, oral anomalies (such as cleft
Toriello–Carey_syndrome
Medical condition
syndrome include several facial disorders, including hypertelorism and telecanthus, epicanthal folds, downslanting palpebral fissures, ptosis, a broad nasal
Seaver–Cassidy_syndrome
Rare genetic condition involving underdeveloped eyelids
include lack of an eyelid fold, an appearance of widely spaced eyes (telecanthus), low nose bridge and ear malformations (including cupping and incomplete
Blepharophimosis, ptosis, epicanthus inversus syndrome
Blepharophimosis,_ptosis,_epicanthus_inversus_syndrome
Medical condition
anomalies associated with hypoplasia of the midface, hypertelorism, telecanthus, maxillary hypoplasia, short nasolabial fold, thin upper lip and larger
Axenfeld–Rieger_syndrome
Medical condition
severe intellectual disability and similar facial features including telecanthus, drooping eyelids, downslanting, short palpebral fissures, a prominent
2p15-16.1 microdeletion syndrome
2p15-16.1_microdeletion_syndrome
syndrome Alagille–Watson syndrome (AWS) Alar nasal cartilages coloboma of telecanthus Albers–Schonberg disease Albinism Albinism deafness syndrome Albinism
List_of_diseases_(A)
List of medical conditions involving craniosynostosis
C1861380)". www.ncbi.nlm.nih.gov. Retrieved 2023-07-06. "Syndactyly-telecanthus-anogenital and renal malformations syndrome (Concept Id: C2678045)".
List of conditions with craniosynostosis
List_of_conditions_with_craniosynostosis
Medical condition
cataract and degeneration of the eye with retinal detachment. Facial: telecanthus (an increased distance between the corners of the eye), a median cleft
Frontonasal_dysplasia
Genetic disorder
infections Rib synostosis Scoliosis Small foot Strabismus Tarsal synostosis Telecanthus Upslanted palpebral fissures Broad nasal bridge Vesicoureteral reflux
Cardiospondylocarpofacial syndrome
Cardiospondylocarpofacial_syndrome
Congenital disorder caused by maternal warfarin administration
Development of the eyes is also affected by warfarin. Microphthalmia, telecanthus and strabismus are common signs of fetal warfarin syndrome. The appearance
Fetal_warfarin_syndrome
Birth defect of abnormally large or thick brain folds
seizures atonic seizures Other possible symptoms of lissencephaly include telecanthus, estropia, hypertelorism, varying levels of intellectual disability,
Pachygyria
Bony ridge on the orbital surface of the lacrimal bone
Carreño, Andrés Parra; Serna, Daniel Restrepo (October 2019). "Traumatic Telecanthus and Posterior Lacrimal Crest Avulsion in a Six-Year-Old Child". Journal
Posterior_lacrimal_crest
Protein-coding gene in the species Homo sapiens
seen in DS, including psychomotor retardation, Strabismus, Epicanthus, Telecanthus, carp-shaped upper lip, low-set dysmorphic ears, and cardiac defects
DSCAM
Medical condition
include: hypertelorism (unusually wide-set eyes, sometimes reported as telecanthus), narrow palpebral fissures (the separation between the upper and lower
Malpuech facial clefting syndrome
Malpuech_facial_clefting_syndrome
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