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279 Possible Causes for Enamel Hypoplasia, Sparse Eyelashes

  • Rapp-Hodgkin Syndrome

    Oral manifestations included hypodontia, microdontia, unerupted mandibular premolars with well formed roots, large dental pulp spaces, enamel hypoplasia, multiple caries,[] hypoplasia (thin or absent tooth enamel) and dysplastic (misshapen or absent) nails.[] […] by anhidrotic ectodermal dysplasia, cleft lip and palate, and accompanied by a characteristic facies (narrow nose and small mouth); wiry, slow-growing, uncombable hair; sparse[]

  • Dyskeratosis Congenita

    eyelashes 16.1 Hyperhiderosis 15.3 Malignancy 9.8 Intrauterine growth retardation 7.6 Liver disease/peptic ulceration/enteropathy 7.3 Ataxia/cerebellar hypoplasia 6.8 Hypogonadism[] Keratinization of the lid margins, absent lacrimal puncta, trichiasis, cicatrizing conjunctivitis, entropion, ectropion, blepharitis, sparse eyelashes, and symblephara are[] […] developmental 25.4 delay/mental retardation Pulmonary disease 20.3 Short stature 19.5 Extensive dental caries/loss 16.9 Oesophageal stricture 16.9 Premature hair loss /greying/sparse[]

  • Hallermann-Streiff Syndrome

    hypoplasia) hypotrichosis, various ophthalmic disorders (e.g. congenital cataracts, bilateral microphthalmia, ptosis, nystagmus) and atrophy of skin (especially around the[] His ophthalmic features included sparse eyelashes and eyebrows, microphthalmia, nystagmus, lower lid entropion in the right eye, and upper lid entropion with blepharoptosis[] […] and thin eyebrow Thin, sparse eyebrows 0000535 Sparse eyelashes Scant eyelashes Scanty eyelashes Thin eyelashes [ more ] 0000653 Telecanthus Corners of eye widely separated[]

  • Oculo-Osteo-Cutaneous Syndrome

    1 Aarskog syndrome ablepharon macrostomia syndrome Abuse Dwarfism Syndrome achondroplasia acromesomelic dysplasia ADULT syndrome Alaninuria with Microcephaly, Dwarfism, Enamel[] 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[] Hypoplasia and Nail Defects Hypertrichosis, Congenital Generalized, With or Without Gingival Hyperplasia Hypohidrotic Ectodermal Dysplasia with Hypothyroidism and Agenesis[]

  • Hidrotic Ectodermal Dysplasia

    The patient presented with mild dysmorphy, severe enamel hypoplasia and hypodontia. The radiograph revealed retained teeth at different stages of development.[] , 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[] Robinson GC, Miller JR, Worth HM (1966) Hereditary enamel hypoplasia: its association with characteristic hair structure. Pediatrics 37:498–502 PubMed Google Scholar 20.[]

  • Singleton Merten Syndrome

    主要主题词: Aortic Diseases; DEAD-box RNA Helicases; Dental Enamel Hypoplasia; Glaucoma; Metacarpus; Models, Molecular; Muscular Diseases; Odontodysplasia; Osteoporosis; Vascular[] eyelashes Cutis laxa Accelerated skeletal maturation Proportionate short stature Elbow flexion contracture Bowing of the long bones Sparse and thin eyebrow Thin skin Sparse[] (focal dermal hypoplasia) (hypodontia; enamel hypoplasia; delayed eruption; malformed teeth; irregular placement) 23. Hajdu-Cheney S.[]

  • Lenz-Majewski Syndrome

    […] a skin condition characterized by hyperostosis, craniodiaphyseal dysplasia, dwarfism, cutis laxa, proximal symphalangism, syndactyly, brachydactyly, mental retardation, enamel[] […] scalp hair Clumsiness Gynecomastia Long eyelashes Horizontal nystagmus Downslanted palpebral fissures Hypogonadotrophic hypogonadism Retinal atrophy Progressive gait ataxia[] hypoplasia and hypertelorism.[]

  • Bloch Sulzberger Syndrome

    Hair changes include vertex alopecia and sparse eyebrows and eyelashes.[] Sparse eyelashes and eyebrows are also reported. Teeth.[]

  • Pfeiffer-Palm-Teller Syndrome

    A syndrome of short stature, amimic facies, enamel hypoplasia, slowly progressive stiffness of the joints, and high-pitched voice in two siblings. J.[] eyelashes Low anterior hairline Postnatal microcephaly Hypertrichosis High myopia Sparse scalp hair Wide nose Thin skin Sparse and thin eyebrow Bowing of the long bones Arthrogryposis[] Pfeiffer-Palm-Teller syndrome is a very rare dysmorphic syndrome described in two sibs and characterized by a short stature, unique facies, enamel hypoplasia, progressive[]

  • Oculodentodigital Dysplasia

    Described here is the case of a 10-year-old girl with enamel hypoplasia, typical facies and mental delay, initially thought to be related to an unknown metabolic disorder.[] […] hair Hypermetropia Recurrent fractures Abnormality of the skin Scarring Thin skin Osteolysis Wormian bones Hyperostosis Sparse eyelashes Fibroma Median cleft lip Single median[] hypoplasia and odontodysplasia.[]

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