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262 Possible Causes for Congenital Eye Anomaly, Sparse Eyelashes

  • Hallermann-Streiff Syndrome

    His ophthalmic features included sparse eyelashes and eyebrows, microphthalmia, nystagmus, lower lid entropion in the right eye, and upper lid entropion with blepharoptosis[] Hallermann-Streiff syndrome is a rare congenital disorder characterized as a complex association of developmental anomalies involving structures of ectodermal origin (the[] […] and thin eyebrow Thin, sparse eyebrows 0000535 Sparse eyelashes Scant eyelashes Scanty eyelashes Thin eyelashes [ more ] 0000653 Telecanthus Corners of eye widely separated[]

  • Anophthalmos

    Facial features can include flattened midface, sparse eyelashes, short palpebral fissures, high palate and cleft lip.[] Four children with severe congenital eye anomalies are described of which three had related symptoms.[] eyelashes Hypertelorism Preauricular skin tag Recurrent pneumonia Tetralogy of Fallot Underdeveloped nasal alae Hypoplasia of the maxilla Low-set, posteriorly rotated ears[]

  • Hydrophthalmos

    He had been diagnosed with hypohidrotic ectodermal dysplasia in childhood, based on sparse, fine hair, brow and eyelashes hypotrichosis, poor tolerance to heat due to low[] Megalocornea with glaucoma Q15.8 Other specified congenital malformations of eye Q15.9 Congenital malformation of eye, unspecified Inclusion term(s): Congenital anomaly of[] Axenfeld anomaly Axenfelds anomaly Axenfelds anomaly (eye condition) Bilateral congenital glaucoma Buphthalmos of left eye Buphthalmos of right eye Glaucoma of childhood[]

  • Hidrotic Ectodermal Dysplasia

    , pale scalp hair short, sparse eyelashes sparse axillary and pubic hair Clinical features from OMIM: 601375 Human phenotypes related to Ectodermal Dysplasia, Hidrotic, Christianson-Fourie[] AEC syndrome (also known as Hay-Wells syndrome) is defined by ankyloblepharon (congenital adhesions between the eyelids) and other eye findings, skin erosions especially of[] Underdeveloped Thick, discolored Hair Fine, brittle, slow-growing Total balding (alopecia) Missing in spots for males Sparse eyelashes Sparse eyebrow Absent underarm hair[]

  • Choroidal Coloboma

    300864 CEREBROOCULOFACIOSKELETAL SYNDROME/Cataracts, blepharophimosis, microphthalmia, nystagmus, deep-set eyes/AR/ERCC6 /#214150 CEREBROOCULONASAL SYNDROME/Anophthalmia, Sparse[] Discussion: Ocular coloboma is a rare congenital anomaly that has a prevalence of around 0.14% in the general population.[] […] in an eyelid. coloboma Congenital, pathological or operative anomaly in which a portion of the structure of the eye is lacking, e.g. coloboma of the choroid, coloboma of[]

  • Oculo-Osteo-Cutaneous Syndrome

    eyelashes 32 HP:0000653 10 anodontia 32 HP:0000674 11 hypotrichosis 32 HP:0001006 12 short toe 32 HP:0001831 13 fine hair 32 HP:0002213 14 absent axillary hair 32 HP:0002221[] Eye Anomalies), Type A, 4 Muscular Dystrophy-Dystroglycanopathy ( Congenital With Brain And Eyeanomalies), Type A, 5 Muscular Dystrophy-Dystroglycanopathy ( Congenital With[] Sparse eyelashes MedGen UID: 375151 • Concept ID: C1843300 • Finding Decreased density/number of eyelashes.[]

  • Isolated Congenital Sclerocornea

    eyelashes Short ribs Rhizomelia Hypopigmentation of the skin Gingival overgrowth Bowing of the long bones Sparse and thin eyebrow Abnormality of retinal pigmentation Abnormality[] A congenital anomaly in which the whole or part of the cornea is opaque and resembles the sclera; other ocular abnormalities are frequently present. sclerocornea /scle·ro·[] 300864 CEREBROOCULOFACIOSKELETAL SYNDROME/Cataracts, blepharophimosis, microphthalmia, nystagmus, deep-set eyes/AR/ERCC6 /#214150 CEREBROOCULONASAL SYNDROME/Anophthalmia, Sparse[]

  • FLOTCH Syndrome

    Symptoms related to Sparse eyelashes include: Woolly hair Sparse hair Sparse or absent eyelashes Sparse lower eyelashes • • • Back to: « Sparse eyelashes Related Symptom Articles[] […] dystrophy congenital infantile cataract hypogonadism Muscular dystrophy congenital, merosin negative Muscular dystrophy, facioscapulohumeral Muscular dystrophy Hutterite[] :0000613 2 abnormality of the nail 60 33 hallmark (90%) Very frequent (99-80%) HP:0001597 3 neoplasm of the skin 60 33 hallmark (90%) Very frequent (99-80%) HP:0008069 4 sparse[]

  • Nestor-Guillermo Progeria Syndrome

    […] and thin eyebrow ; Sparse eyelashes ; Spotty hyperpigmentation ; Wide cranial sutures Associated Genes BANF1 (Withdrawn symbols: BAF ) Mouse Orthologs Banf1 (Withdrawn symbols[] […] with brain and eye anomalies A11 (MDDGA11) [MIM: 615181 ] B3GAT3 O94766 non-pleiotropic Multiple joint dislocations short stature craniofacial dysmorphism and congenital[] BANF1 gene alterations may also develop some of the following symptoms and phenotypes: Commonly - More than 50% cases Osteolysis Not very common - Between 30% and 50% cases Sparse[]

  • Mandibulofacial Dysostosis

    People with Treacher Collins syndrome often have eyes that slant downward, sparse eyelashes, and a notch in the lower eyelids called an eyelid coloboma.[] Anterior Chamber Brain Choroid Congenital Syndromes Albinism (see under Iris) Anomalies of Eye Size Chromosomal Anomalies Malformation of the Optic Cup Marcus Gunn Jaw-Winking[] eyelashes, and a notch in the lower eyelids called an eyelid coloboma.[]

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