Create issue ticket

47 Possible Causes for Congenital Alopecia, Facial Hemiatrophy

  • Alopecia

    Congenital triangular alopecia Congenital triangular alopecia references Congenital triangular alopecia Congenital triangular alopecia is a patch of hair loss in the temple[keratin.com] Despite the low prevalence, congenital alopecia areata is an important differential diagnosis for neonatal hair loss.[ncbi.nlm.nih.gov] A breach in this immune privilege state is considered as the cause of alopecia areata. [4] A few cases of babies being born with congenital alopecia areata have been reported[en.wikipedia.org]

  • Sclerodactyly

    Abstract A Japanese woman was diagnosed as having progressive facial hemiatrophy when she was 26 years old.[link.springer.com] The main manifestations are total congenital alopecia, bilateral congenital cataracts, and skin changes of the hands and feet including sclerodactyly, hyperkeratosis, contractures[ncbi.nlm.nih.gov] Get Update Overview Palmoplantar keratoderma and congenital alopecia-2 (PPKCA2) is an autosomal recessive disorder characterized by congenital alopecia and progressive hyperkeratosis[diseaseinfosearch.org]

  • Cerebellotrigeminal Dermal Dysplasia

    hemiatrophy (Parry-Romberg syndrome) Linear scleroderma (morphoea) en coup de sabre Unilateral somatic and intracranial hypoplasia Oculocerebrocutaneous syndrome (Delleman[chipsbooks.com] alopecia of a zone of the occipital and posterior parietal scalp is presented.[ncbi.nlm.nih.gov] hemiatrophy (parry-romberg syndrome) -- Linear scleroderma (morphoea) “en coup de sabre” -- Unilateral Somatic and Intracranial Hypoplasia -- Oculocerebrocutaneous Syndrome[library.jkuat.ac.ke]

  • Tollner-Horst-Manzke Syndrome

    Abnormalities, Kyphoscoliosis, and Mental Retardation Facial Dysmorphism, Hypertrichosis, Epilepsy, Intellectual/Developmental Delay, and Gingival Overgrowth Syndrome facial[rgd.mcw.edu] alopecia Autosomal dominant partial epilepsy with auditory features Autosomal dominant polycystic kidney disease - Not a rare disease Autosomal dominant pseudohypoaldosteronism[rarediseases.info.nih.gov] hemiatrophy Facio Thoraco Genital Syndrome Faciocardiomelic Syndrome Faciocardiorenal Syndrome factitious disorder Failed Back Surgery Syndrome Fallot Complex with Severe[rgd.mcw.edu]

  • Ectropion

    Although EU has been associated with several systemic diseases, including neurofibromatosis, facial hemiatrophy, and Prader-Willi syndrome, the condition is most often associated[aao.org] Congenital ichthyosis with alopecia, eclabion, ectropion and mental retardation--a new genetic syndrome. Clin. Genet. 31: 102-108, 1987.[omim.org] Oligophrenia in combination with congenital ichthyosis and spastic disorders: a clinical and genetic study. Acta Psychiat. Neurol. Scand. 113 (suppl.): 1-113, 1957.[omim.org]

  • Rasmussen Syndrome

    Parry-Romberg syndrome (progressive facial hemiatrophy) is a unilateral, slowly progressive atrophy affecting the skin, subcutaneous tissues, muscles, and bones.[ncbi.nlm.nih.gov] A 9-year-old boy diagnosed as having Rasmussen syndrome had congenital IgA deficiency and juvenile alopecia.[ncbi.nlm.nih.gov] We report the clinical and neuroradiological findings in a 6-year-old boy, presenting with focal hemifacial and arm motor seizures and progressive facial hemiatrophy.[ncbi.nlm.nih.gov]

  • Salti-Salem Syndrome

    hemiatrophy Facio Thoraco Genital Syndrome Faciocardiomelic Syndrome Faciocardiorenal Syndrome factitious disorder Failed Back Surgery Syndrome Familial Antiphospholipid[rgd.mcw.edu] Alopecia X-Linked Congenital Infantile Muscular Dystrophy with Cataract and Hypogonadism Cutaneous Telangiectasia and Cancer Syndrome, Familial De Sanctis-Cacchione Syndrome[rgd.mcw.edu] Alopecia congenita keratosis palmoplantaris 0 *Alopecia/congenital *Keratoderma, Palmoplantar. Total Hypotrichosis, Mari type 0 *Alopecia/congenital.[reference.md]

  • Skin Atrophy

    hemiatrophy.[blackwellreference.com] Scarring alopecia, congenital absence of three toenails, and a scarlike lesion of the tongue were also present.[ncbi.nlm.nih.gov] […] borreliosis) 6 Follicular atrophoderma 7 Vermiculate atrophoderma 8 Atrophoderma of Pasini and Pierini (probably morphoea) 9 Atrophic naevi 10 Panatrophy: (a) local panatrophy (b) facial[blackwellreference.com]

  • Phakomatosis Pigmentokeratotica

    Pascual-Castroviejo Progressive facial hemiatrophy I. Pascual-Castroviejo Unilateral facial and intracranial hypoplasia[hoepli.it] Alopecia Syndrome Other Disorders of Keratinization Porokeratoses Kyrle’s Disease Pityriasis Rubra Pilaris Poikilodermas and Aging Syndromes Disorders of DNA Repair Aging[routledge.com] Pascual-Castroviejo Progressive facial hemiatrophy I. Pascual-Castroviejo Unilateral facial and intracranial hypoplasia.[searchworks.stanford.edu]

  • CANOMAD Syndrome

    hemiatrophy En coup de sabre Systemic sclerosis (Scleroderma): Subtypes Diffuse cutaneous scleroderma Rapidly progressive Widespread skin thickening Similar syndromes 2 toxins[neuromuscular.wustl.edu] […] choroidal dystrophy Chorioretinitis Chorioretinopathy dominant form microcephaly Choroid plexus carcinoma Choroid plexus cyst Choroid plexus papilloma Choroidal atrophy alopecia[herenciageneticayenfermedad.blogspot.com] Azathioprine: Corticosteroid sparing agent Scleroderma Types Localized scleroderma Morphea: Plaques of skin fibrosis Linear scleroderma: Bands of fibrosis; May be associated with facial[neuromuscular.wustl.edu]

Further symptoms

Similar symptoms