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36 Possible Causes for Hypertrichosis of Eyebrows, Neurologic Symptoms Are Progressive

  • Alpha-Mannosidosis

    ICD-9: 278.8 ONSET AND PROGRESSION Type III alpha mannosidosis is the most severe form, and signs and symptoms appear in infancy with rapid progression, severe neurological[] Signs and symptoms of the disease may vary from mild to severe. Alpha Mannosidosis may appear in childhood with rapid progression and severe neurological impairment.[] Affected individuals often appear normal at birth but eventually develop progressive neurologic symptoms including sensory and motor deficits, mental retardation, and seizures[]

  • Coffin-Lowry Syndrome

    Complications resulting in early death include spinal stenosis leading to neurologic symptoms, and progressive kyphoscoliosis leading to impaired cardiorespiratory function[]

  • Fucosidosis

    Early onset and rapid progression of neurological symptoms. 2.Skin changes compatible with angiokeratoma corporis diffusum. 3.[] The disease will normally progress rapidly with neurological symptoms and is often fatal before the sixth year of life.[] Currently, there is no cure to stop the progression of symptoms of Fucosidosis and treatment is aimed at addressing the individual problems as they arise.[]

  • Autosomal Recessive Deafness 88

    […] of eyebrows; 4. white forelock; 5. heterochromia of irides; 6.[] […] presents w/episodic or progressive ataxia & progressive sensorineural deafness neurologic or cutaneous symptoms, consider biotinidase deficiency.[] The neurological symptoms usually include focal epilepsy, migraine, and unilateral brain lesions on the same side as the atrophy.[]

  • Autosomal Dominant Prognathism

    […] congenita terminalis (thick scalp hair extending onto the forehead with generalized increased body hair) associated with a typical acromegaloid facial appearance (thick eyebrows[] Symptoms INHERITANCE: Autosomal dominant NEUROLOGIC: [Central nervous system]; Dementia, rapidly progressive; Personality changes; Parkinsonian symptoms; Spongiform changes[] APPEARANCE SYNDROME Hypertrichosis-acromegaloid facial appearance syndrome (HAFF) is a very rare multiple congenital abnormality syndrome manifesting from birth with progressive hypertrichosis[]

  • Hepatoerythropoietic Porphyria

    Hypertrichosis of temporal and malar facial areas is often observed. Heavier growth of eyebrow, beard and limb hair may also occur. Figure 1.[] In rare cases, neurological symptoms such as progressive polyneuropathy have been reported. Treatment Options Treatment options are summarized in Table I . Table I.[]

  • Qazi-Markouizos Syndrome

    The coarse facial features and hypertrichosis of the eyebrows may not be present at birth but may develop after early infancy.[] […] diseases and genetic alterations Myopia and Progressive neurologic deterioration, related diseases and genetic alterations Brachydactyly and Ventricular hypertrophy, related[] Learn more about how to achieve it with Mendelian Learn more Other signs and symptoms that you may find interesting Downslanted palpebral fissures and Babinski sign, related[]

  • Acrootoocular Syndrome

    A down sloping V-shaped configuration of the eyebrows as they met and extended onto the upper part of the nasal bridge is common. Brow hypertrichosis may be observed.[] Familial idiopathic basal ganglia calcification (Fahr’s disease) without neurological, cognitive and psychiatric symptoms is not linked to the IBGC1 locus on chromosome 14q[] Non-progressive familial idiopathic intracranial calcification: a family report.[]

  • Autosomal Dominant Mental Retardation Type 21

    […] that grow together (synophrys); long, curly eyelashes; and/or excessive hair growth on various areas of the body (hypertrichosis).[] Human immunodeficiency virus encephalopathy was characterized by microcephaly, progressive neurological deterioration, mental retardation, cerebellar symptoms, and behavioral[] The affected individuals had no dysmorphic features, neurological symptoms, or epilepsy, and head circumference was normal in all but one patient.[]

  • Acrorenal Mandibular Syndrome

    Sparse and thin eyebrow Small nail Large fontanelles Enlarged cochlear aqueduct Dilatated internal auditory canal Incomplete partition of the cochlea type II Atresia of the[] Learn more about how to achieve it with Mendelian Learn more Other signs and symptoms that you may find interesting Hyperreflexia and Progressive neurologic deterioration,[] […] impairment Abnormal lacrimal duct morphology Focal seizures with impairment of consciousness or awareness Schizophrenia Horizontal nystagmus Recurrent urinary tract infections Hypertrichosis[]

Further symptoms