Create issue ticket

1,757 Possible Causes for Flat Affect, Round Face in Infancy, Umbilical Plaque

  • Weaver Syndrome

    Although both sexes are affected, the sex ratio is 2M:1F.[] Craniofacial: macrocephaly, flat occiput, redundant nuchal skin folds, broad forehead with frontal bossing, thin scalp hair, hypertelorism, upslanting or downslanting palpebral[]

  • Umbilical Hernia

    A tailored flat Surgisis graft was used to ensure an overlap of at least 2 cm; in all patients the mesh was fixed by fibrin glue.[] METHODS: Thirty-six consecutive patients, mean age 45.25 /- 12.19 years, affected by primary umbilical uncomplicated hernia with a defect size or 3 cm, were treated in a day-surgery[]

    Missing: Round Face in Infancy
  • Endometriosis

    His affect is flat. Which of the following is the most appropriate pharmacotherapy?[]

    Missing: Round Face in Infancy
  • Adenocarcinoma of the Colon

    In these conditions, both tendons can be affected foot problems – some people with flat feet or hyperpronated feet (feet that turn inward while walking) are prone to Achilles[]

    Missing: 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[] […] and round cheeks, small hands and feet with bilateral brachymetaphalangism, proximal implantation of the thumbs and short toenails, mild mental retardation and autistic behaviour[]

    Missing: Umbilical Plaque
  • Hypertelorism

    He had abnormally wide set eyes, a flat facial appearance and a deformed cleft nose. The distance between his eyes was 50 mm.[] His very wide set eyes were affecting his normal vision (like bird’s vision). He was referred to Balaji Dental & Craniofacial Hospital for specialized face surgery. Dr.[]

    Missing: Round Face in Infancy
  • Mucopolysaccharidosis 6

    The affected individuals often suffer from pain, gait difficulties, and restriction of joint movement.[] Examples include low and flat nasal bridge, frontal bossing, gingival hypertrophy, macroglossia, and hirsutism.[] Patients present with short stature, flat nasal bridge, and joint findings. Urine GAGs are normal in MPS IX.[]

    Missing: Round Face in Infancy
  • Mucopolysaccharidosis 1

    Patients present with short stature, flat nasal bridge, and joint findings. Urine GAGs are normal in MPS IX.[] The eye's cornea often becomes cloudy from intracellular storage, and glaucoma and degeneration of the retina also may affect the patient's vision.[] MPS VII is extremely rare, affecting approximately 1 in 1,500,000 individuals. MPS IX is a very rare disorder caused by a deficiency of the enzyme hyaluronidase.[]

    Missing: Round Face in Infancy
  • Baraitser-Winter Syndrome 1

    The face is round and flat in infancy.[] The median part of the face is broad with a wide nasal base and marked hypertelorism (39/41–95%).[]

    Missing: Flat Affect
  • Fetal Hydantoin Syndrome

    In this infant note the narrow sloping forehead, flat depressed nasal bridge, mild micrognathia, and microtia with absence of the external auditory canal.[] Affected infants may have hydrocephalus, microcephaly, or thymic abnormalities. This mother was treated with retinoic acid during the first month of pregnancy.[]

    Missing: Round Face in Infancy