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26 Possible Causes for Flat Affect, Hearing Impairment, Round Face in Infancy

  • Autism

    Her clinical features included hypotonia and feeding difficulties during infancy, coarse face with notably prominent forehead, prominent eyebrows, broad flat nasal bridge[] Your child will undergo a formal audiological assessment where he or she is tested for any hearing impairments, as well as any other hearing issues or sound sensitivities[] Visual impairment; hearing impairment.[]

  • Char Syndrome

    Note the round face with full cheeks, hypertelorism, epicanthal folds, and apparently low-set ears. Child with cri-du-chat syndrome.[] Other symptoms such as vision problems, hearing impairment and developmental delay are treated using routine methods.[] A, Typical facial features of Char syndrome in an affected 46-year-old woman from the Arkansas family.[]

  • Goldberg-Shprintzen Syndrome

    In infancy, there are excess nuchal skin, a rounded skull shape, a sparse fine hair and a puffy anterior neck; the face is square shaped with high forehead, frontal bossing[] The main skeletal findings in SGS are arachnodactyly, flat feet, pectus deformity, scoliosis and hypermobile joints [ 1 ].[] An audiological evaluation should be performed in all children with language impairment, including MWS patients [ 19, 34 ].[]

  • Wolf-Hirschhorn Syndrome

    Microcephaly Round, moonlike face Wide-set, downward-slanting eyes Strabismus Epicanthal folds Williams syndrome Type of abnormality: deletion Critical region: 7q11.23 Mental[] More than 25 genes for nonsyndromic hereditary hearing impairment have been mapped.[] Most individuals affected by this disorder have distinctive facial features, such as a broad, flat nasal bridge and a high forehead described as the “Greek warrior helmet”[]

  • Cutaneous Mastocytosis - Short Stature - Conductive Hearing Loss - Microtia

    Craniofacial features: i. round face in infancy, ii. a prominent forehead (70%), iii. hypertelorism (76%), iv. narrow palpebral fissures (79%), v. a long philtrum (91%), vi[] In one of these patients, hearing impairment was aggravated by concurrent sensorineural hearing loss.[] , broad and flat nasal bridge, and low-set ears), renal anomalies (nephromegaly and hydronephrosis), frequent neurodevelopmental delay, and high neonatal mortality.[]

  • Optic Atrophy-Intellectual Disability Syndrome

    Affected individuals also have distinctive facial features, including widely set eyes (hypertelorism), low-set ears, a small jaw, and a rounded face.[] A brain MRI, recommended at age three or older A full, dilated eye examination by an ophthalmologist every two years A full hearing evaluation every two years A comprehensive[] Most affected individuals have facial features described as coarse.[]

  • Disproportionate Short Stature - Ptosis - Valvular Heart Lesions

    50–65 ASD, VSD, PDA, LSVC, aortic atresia, dextrocardia, TOF, tricuspid atresia 22, 154 Deletion 5p (cri-du-chat) Catlike cry, prenatal and postnatal growth retardation, round[] impairment Sensorineural hearing impairment Depressed nasal bridge Wide nasal bridge Macrocephaly Anteverted nares Congenital onset Micropenis Oxycephaly Abnormality of the[] Symptoms and Signs Affected neonates tend to be placid, rarely cry, and have hypotonia.[]

  • Thyro-Cerebro-Renal Syndrome

    Affected individuals also have distinctive facial features, including widely set eyes (hypertelorism), low-set ears, a small jaw, and a rounded face.[] Related symptoms: Autosomal recessive inheritance Global developmental delay Short stature Hearing impairment Microcephaly SOURCES: UMLS MONDO OMIM More info about SHORT STATURE[] The head may appear flat at the top (vertex) and back (occiput).[]

  • Cole-Carpenter Syndrome

    Round face Wide anterior fontanel Rhizomelia Coxa vara Relative macrocephaly Thoracolumbar scoliosis Feeding difficulties Breech presentation Lumbar scoliosis Dentinogenesis[] An individual affected by the syndrome may have broad cheeks, a flat nasal bridge, and a wide upturned nose with abnormally large nasal openings.[] Some affected individuals also have dental abnormalities including small primary (baby) teeth. Vision problems also frequently occur.[]

  • Congenital Non-Progressive Ataxia

    Affected individuals also have distinctive facial features, including widely set eyes (hypertelorism), low-set ears, a small jaw, and a rounded face.[] Three patients have hearing impairment (3/9; 33%).[] For example, affected individuals have exhibited skeletal malformations, such as fusion of certain bones in the spinal column of the neck (cervical vertebrae), flat feet ([]

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