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355 Possible Causes for Thick Eyebrows

  • Wiedemann-Steiner Syndrome

    Humangenetik der Johann Wolfgang Goethe Universität, Frankfurt, Germany. [email protected] Abstract We describe three patients with a syndrome comprising arched, thick[] Wiedemann-Steiner syndrome (WSS) is an autosomal dominant congenital anomaly syndrome characterized by hairy elbows, dysmorphic facial appearances (hypertelorism, thick eyebrows[] eyebrows).[]

  • Coffin-Lowry Syndrome

    eyebrows.[] eyebrows Skeletal abnormalities may include: Abnormal front-to-back and side-to-side curvature of the spine (kyphoscoliosis) Unusual prominence of the breastbone (pigeon[] […] protruding nostrils (nares), an abnormally prominent brow, downslanting eyelid folds (palpebral fissures), widely spaced eyes (hypertelorism), large ears, and unusually thick[]

  • Rubinstein-Taybi Syndrome

    eyebrow Bushy eyebrows Dense eyebrow Heavy eyebrows Prominent eyebrows Thick eyebrows [ more ] 0000574 Truncal obesity 0001956 Unsteady gait Unsteady walk 0002317 Variable[] Specific growth charts for monitoring growth in individuals with RSTS have now been developed. [ 6 ] Facial features: low frontal hairline, arched thick eyebrows, downslanting[] Arched eyebrows Broad, arched eyebrows High, rounded eyebrows High-arched eyebrows Thick, flared eyebrows [ more ] 0002553 Irritability Irritable 0000737 Microcephaly Abnormally[]

  • Tenorio Syndrome

    eyebrow Anxiety Delayed speech and language development Osteopenia Hypertrichosis Keratoconjunctivitis sicca Intellectual disability Seizures Muscular hypotonia Syncope .[] eyebrow Hepatomegaly Macroglossia Hypertrichosis Clumsiness Conjunctivitis Delayed cranial suture closure Keratitis Keratoconjunctivitis sicca Large forehead Recurrent aphthous[] Syndrome : Autosomal dominant inheritance Macroglossia Hydrocephalus Macrocephaly Delayed cranial suture closure Mandibular prognathia Wide nose Anteverted nares Telecanthus Thick[]

  • Waardenburg Syndrome, Type 1

    Partial albinism ; Premature graying of hair ; Smooth philtrum ; Spina bifida ; Sprengel anomaly ; Supernumerary ribs ; Supernumerary vertebrae ; Synophrys ; Telecanthus ; Thick[] eyebrow ; Underdeveloped nasal alae ; White eyebrow ; White eyelashes ; White forelock ; Wide nasal bridge Associated Genes PAX3 (Withdrawn symbols: HUP2, WS1 ) Mouse Orthologs[]

  • Kondoh Syndrome

    eyebrow 33 HP:0000574 6 short stature 33 HP:0004322 7 long philtrum 33 HP:0000343 8 intrauterine growth retardation 33 HP:0001511 9 thin upper lip vermilion 33 HP:0000219[] eyebrows Head And Neck Mouth: thin upper lip Skeletal Limbs: knee contracture Skeletal Hands: polydactyly, preaxial interphalangeal joint contractures Head And Neck Head:[] […] finger 33 HP:0001220 Symptoms via clinical synopsis from OMIM: 58 Head And Neck Eyes: ptosis Growth Height: short stature Skin Nails Hair Hair: sparse hair widow's peak thick[]

  • Marshall-Smith Syndrome

    eyebrow Bushy eyebrows Dense eyebrow Heavy eyebrows Prominent eyebrows Thick eyebrows [ more ] 0000574 Umbilical hernia 0001537 Showing of 75 Last updated: 3/1/2019 While[] […] philtrum 0000322 Short sternum 0000879 Sporadic No previous family history 0003745 Synophrys Monobrow Unibrow [ more ] 0000664 Tall stature Increased body height 0000098 Thick[]

  • Alpha-Mannosidosis

    Eyebrows appear thick. Systemic Features: Mannosidosis is a highly variable multisystem disorder.[]

  • Coffin-Siris Syndrome

    Abstract We report a white female infant with typical features of Coffin-Siris syndrome including thick eyebrows, flat nasal bridge, anteverted, wide nose tip, generalised[] Cardinal features of CSS included variable degrees of intellectual disability (ID) predominantly affecting speech, sucking/feeding difficulty, and craniofacial (thick eyebrows[] Typical CSS facies exhibit a wide mouth and nasal bridge, everted lips, downward slanting eyes, and thick eyebrows.[]

  • Cerebro-Facio-Thoracic Dysplasia

    Abstract We report a further two patients with cerebro-facio-thoracic dysplasia, a rare autosomal recessive condition with thoracic costovertebral dysplasia, developmental delay and characteristic facial features. One of our patients has the additional features of large, bilateral colobomas of the optic nerve,[…][]

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