Create issue ticket

143 Possible Causes for Triangular Facies

  • Woodhouse Sakati Syndrome

    BACKGROUND AND OBJECTIVE: Woodhouse-Sakati syndrome (WSS) is a rare autosomal-recessive disorder characterized by a combination of hypogonadism, alopecia, diabetes mellitus (DM), mental retardation and extrapyramidal signs, not described previously in Israel. Our aim was to study the clinical and genetic[…][]

  • Russell-Silver Syndrome

    Abstract Russell-Silver syndrome, a syndrome of unknown etiology, is characterized by short stature of prenatal onset, triangular facies, asymmetry, variations in the pattern[] Russell-Silver syndrome (RSS) is a disorder characterized by pre- and post-natal growth deficiency, triangular facies, relative macrocephaly, and body asymmetry.[] Abstract Russell-Silver syndrome (RSS) is characterized by prenatal and postnatal growth retardation, triangular facies, and fifth-finger clinodactyly.[]

  • Ring Chromosome 15

    Russell-Silver and ring 15 syndromes share clinical features such as growth deficiency, triangular facies, digital anomalies, and café-au-lait spots.[] The main characteristics of this syndrome include growth retardation (100%), variable mental retardation (95%), microcephaly (88%), hypertelorism (46%), and triangular facies[] The girls also had growth retardation, microcephaly, hypertelorism, triangular facies, and a 46,XY, r(15) karyotype.[]

  • Benign Migratory Glossitis

    Robinow's syndrome or fetal facies syndrome is a rare genetic disorder and includes a series of anomalies such as short stature, characteristic facial dysmorphism (fetal facies[] Cerqueira and de Souza described the orofacial manifestations of the Robinow's syndrome which included: triangular mouth and a long upper lip philtrum, ankyloglossia, a shortened[]

  • Cataract

    She had a triangular facies, a prominent forehead, proptosis, a small nose, and a small jaw.[]

  • SHORT Syndrome

    Definition A rare, multisystem disease characterized by short stature, anomalies of the anterior chamber of the eye, characteristic facial features such as triangular facies[] facies anteverted ears telecanthus deep set eyes wide nasal bridge hypoplastic alae nasi chin dimple micrognathia clinodactyly partial lipodystrophy hearing loss functional[] These are: triangular progeroid facies with a prominent forehead, absence of facial fat, midface hypoplasia, and hypoplastic nasal alae.[]

  • Cutis Laxa

    Patients display facial dysmorphism, with triangular facies and progeroid appearance.[] Figure 1 ( a ) The patient at 8 months with cutis laxa, a broad forehead, triangular facies and adducted thumbs. ( b ) T2-weighted coronal brain MRI at age 3 years showing[]

  • Mulibrey Nanism Syndrome

    facies, broad forehead & low nasal bridge.[] […] face, hypoplastic midface, midface, long philtrum, philtrum, prominent lips, “gloomy gloomy facies” facies[] […] diagnosed with mulibrey nanism predominantly have prenatal growth retardation, failure to thrive, hepatomegaly and characteristic craniofacial features including scaphocephaly, triangular[]

  • Craniorhiny

    facies, and sensorineural hearing loss Cleidocranial Dysplasia COCOON SYNDROME CODAS syndrome Combined Oxidative Phosphorylation Deficiency 2 Congenital Cataracts, Facial[] Facies, and Sensorineural Hearing Loss Cleft Palate, Psychomotor Retardation, and Distinctive Facial Features cleidocranial dysplasia cocoon syndrome CODAS Syndrome Combined[] 2p16.1-P15 Deletion Syndrome Chromosome 2q31.2 Deletion Syndrome CHROMOSOME 8q21.11 DELETION SYNDROME Chromosome Xq28 Duplication Syndrome Cleft palate, midfacial hypoplasia, triangular[]

  • CANOMAD Syndrome

    facies, and sensorineural hearing loss Cleft palate-cardiac defect-genital anomalies-ectrodactyly syndrome - See Acrocardiofacial syndrome Cleft palate-omphalocele syndrome[] […] congenital heart disease, dislocated hips, absent tibiae, bowed fibulae, preaxial polydactyly of the feet, - See Ho Kaufman Mcalister syndrome Cleft palate, midfacial hypoplasia, triangular[]

Further symptoms