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searching for Hypertelorism 25 found (160 total)

Axenfeld–Rieger syndrome (2,709 words) [view diff] exact match in snippet view article find links to article

are craniofacial anomalies associated with hypoplasia of the midface, hypertelorism, telecanthus, maxillary hypoplasia, short nasolabial fold, thin upper

Goldberg–Shprintzen syndrome (1,327 words) [view diff] exact match in snippet view article find links to article

Goldberg and R J Shprintzen in 1982. The sibling pair had microcephaly, hypertelorism, short stature, submucous cleft palate, learning problems, and Hirschsprung

Say–Meyer syndrome (1,026 words) [view diff] exact match in snippet view article find links to article

bones which gives the forehead a triangular shape) Hypotelorism or hypertelorism (reduced or increased width between the eyes) Craniosynostosis (when

Gastrocutaneous syndrome (65 words) [view diff] exact match in snippet view article find links to article

Gastrocutaneous syndrome Other names Peptic ulcer/hiatal hernia, multiple lentigines/cafe-au-lait spots, hypertelorism, myopia Specialty Dermatology

Chromosomal deletion syndrome (1,128 words) [view diff] exact match in snippet view article find links to article

tags, round faces, short neck, micrognathia, and dental malocclusion, hypertelorism, epicanthal folds, downturned corners of the mouth. There is no specific

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

type III Hypersensitivity type IV Hypersomnolence Hypertelorism and tetralogy of Fallot Hypertelorism hypospadias syndrome Hypertension Hypertensive hyperkalemia

List of diseases (I) (577 words) [view diff] exact match in snippet view article

Iophobia Iridocyclitis Iridogoniodysgenesis, dominant type Iris dysplasia hypertelorism deafness Iritis Iron deficiency Iron overload Irons–Bhan syndrome Irritable

CEDNIK syndrome (564 words) [view diff] exact match in snippet view article find links to article

characteristic with elongated faces, antimongolian eye slant, slight hypertelorism and flat broad nasal root. Palmoplantar keratoderma and ichthyosis appears

Santos–Mateus–Leal syndrome (240 words) [view diff] exact match in snippet view article find links to article

"Hirschsprung disease associated with polydactyly, unilateral renal agenesis, hypertelorism, and congenital deafness: a new autosomal recessive syndrome". Journal

List of diseases (T) (849 words) [view diff] exact match in snippet view article

V1 Telangiectasia, hereditary hemorrhagic Telangiectasia Telecanthus hypertelorism pes cavus Telecanthus with associated abnormalities Telencephalic leukoencephalopathy

Donnai–Barrow syndrome (1,218 words) [view diff] exact match in snippet view article find links to article

(1993). "Diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, and sensorineural deafness: a newly recognized autosomal recessive

Weissenbacher–Zweymüller syndrome (685 words) [view diff] exact match in snippet view article find links to article

Typical abnormal facial features can be wide-set protruding eyes (hypertelorism), a small and upturned nose with a flat bridge, small jaw (micrognathia)

7p22.1 microduplication syndrome (326 words) [view diff] exact match in snippet view article find links to article

cranio-facial dysmorphisms such as macrocephaly, frontal bossing, low-set ears, hypertelorism, etc., intellectual disabilities, speech and motor delays, and heart

Children's Surgical Centre (1,136 words) [view diff] exact match in snippet view article find links to article

Gollogly, J; Krishnan, KG; Schackert, G; Lauer, G (2008). "Telecanthus and hypertelorism in frontoethmoidal meningoencephaloceles and the surgical correction

Proboscis (anomaly) (427 words) [view diff] exact match in snippet view article

cribriform plate cells are often missing on this side as well. Ocular hypertelorism (eyes set far apart) may be present. The proboscis lateralis is a rare

Genetic studies on Arabs (6,347 words) [view diff] exact match in snippet view article find links to article

hyperplasia, methyl coenzyme dehydrogenase deficiency;. Teebi type of hypertelorism (1987), Teebi Shaltout syndrome (1989), Al Gazali syndrome (1994), Megarbane

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

index patient was a newborn 46,XX Japanese girl with craniosynostosis, hypertelorism, mid-face hypoplasia, radiohumeral synostosis, arachnodactyly and disordered

Dian Donnai (316 words) [view diff] exact match in snippet view article find links to article

(1993). "Diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, and sensorineural deafness: a newly recognized autosomal recessive

Spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome (991 words) [view diff] exact match in snippet view article find links to article

excavatum, larynx, tracheal, and costal calcifications, frontal bossing, hypertelorism, eye prominence, flat and short nose, wide nostrils, high-arched palate

TAF1 (2,422 words) [view diff] exact match in snippet view article find links to article

palpebral fissures, prominent periorbital ridges, deep-set eyes, relative hypertelorism, thin upper lip, a high-arched palate, prominent ears with thickened

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

stature heart and skeletal anomalies Mental retardation short stature hypertelorism Mental retardation short stature microcephaly eye Mental retardation

SRD5A3-CDG (1,321 words) [view diff] exact match in snippet view article find links to article

movements) of the eyes Abnormal facial shape with deep-set eyes and orbital hypertelorism (increased distance between eyes) Neurological abnormalities that impair

C-Raf (8,674 words) [view diff] exact match in snippet view article find links to article

LEOPARD syndrome (Lentigo, Electrocardiographic abnormalities, Ocular hypertelorism, Pulmonary stenosis, Abnormal genitalia, Retarded growth, Deafness)

C3orf62 (1,233 words) [view diff] exact match in snippet view article find links to article

developmental delay and distinctive facial features (including arched eyebrows, hypertelorism, epicanthus, and micrognathia). In the gene region, NCBI SNP identified

SKIV2L (3,218 words) [view diff] exact match in snippet view article find links to article

with age. These include a large forehead, broad base of the nose and hypertelorism. Overall the facial features are described as “coarse”. Liver disease