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90 Possible Causes for Congenital Alopecia, Facial Hemiatrophy, Werner Syndrome

  • 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]

  • 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] Neurocutaneous lipomas (Krabble-Bartle syndrome) Rhodmund syndrome (including Werner syndrome, Hutchinson-Gilford progeria syndrome) I.[barnesandnoble.com]

  • 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] Syndrome 21 Lipodystrophy Acquired Generalized 143 Werner Syndrome 22 Lipodystrophy Acquired Partial 144 Williams Syndrome 23 Lipodystrophy Congenital Generalized 145 Winchester[books.google.ro]

  • Dilated Cardiomyopathy-Hypergonadotropic Hypogonadism Syndrome

    Although Chen et al. (2003) designated this patient as having 'atypical Werner syndrome' (277700), Hegele (2003) suggested that the patient more likely had late-onset Hutchinson-Gilford[gepedia.com] Abnormalities, Kyphoscoliosis, and Mental Retardation facial hemiatrophy Facio Thoraco Genital Syndrome Faciocardiomelic Syndrome Faciocardiorenal Syndrome factitious disorder[rgd.mcw.edu] […] variant 613454 FOXN1 17q11.2 T-cell immunodeficiency, congenital alopecia, and nail dystrophy 601705 FOXP3 Xp11.23 Immunodysregulation, polyendocrinopathy, and enteropathy[institutobernabeu.com]

  • Congenital Trigeminal Anesthesia

    المحتويات Chapter 25 Werners Syndrome 241 Chapter 26 Progeria 247 Chapter 27 Neuroectodermal Melanolysosomal Disease 254 Chapter 28 RuvalcabaMyhre Syndrome 261 DISEASES WITH[books.google.com] Masticatory spasm in facial hemiatrophy. Ann Neurol 1980;7:585–587. 52. Kim JS, Choi-Kwon S. Sensory sequelae of medullary infarction.[neupsykey.com] Giant congenital triangular alopecia mimicking alopecia areata.[ijtrichology.com]

  • 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] Tht Placebo Syndrome" Pgrllament (Casablanca) Id. "Rumours" Fleetwood Mac (Werner Irot.) IS. "Foot Loot 4 Fancy Free" Nod Stewart IWarntr Bros.) It.[newspapers.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] Pagina 117 - Kyng KJ, May A, Kolvraa S, Bohr VA (2003) Gene expression profiling in Werner syndrome closely resembles that of normal aging.[books.google.ro]

  • Achard Thiers Syndrome

    Abnormalities, Kyphoscoliosis, and Mental Retardation facial hemiatrophy Facio Thoraco Genital Syndrome Faciocardiomelic Syndrome Faciocardiorenal Syndrome factitious disorder[rgd.mcw.edu] Castillo Syndrome Aicardi Syndrome AIDS (Acquired Immune Deficiency Syndrome) AIDS Dysmorphic Syndrome Alagille Syndrome Albinism, Oculocutaneous Alexander Disease Alkaptonuria Alopecia[arrayit.com] Syndrome 21 Lipodystrophy Acquired Generalized 143 Werner Syndrome 22 Lipodystrophy Acquired Partial 144 Williams Syndrome 23 Lipodystrophy Congenital Generalized 145 Winchester[books.google.com]

  • Hallermann-Streiff Syndrome

    Syndrome 21 Lipodystrophy Acquired Generalized 143 Werner Syndrome 22 Lipodystrophy Acquired Partial 144 Williams Syndrome 23 Lipodystrophy Congenital Generalized 145 Winchester[books.google.com] hemiatrophy Facio Thoraco Genital Syndrome Faciocardiomelic Syndrome Faciocardiorenal Syndrome factitious disorder Failed Back Surgery Syndrome Familial Antiphospholipid[rgd.mcw.edu] Synonym: congenital sutural alopecia, hallermann-streiff syndrome, hallermann-streiff-francois syndrome, mandibulo-oculofacial syndrome, oculomandibulodyscephaly, oculomandibulofacial[biology-online.org]

  • Chudley-Rozdilsky Syndrome

    Abnormalities, Kyphoscoliosis, and Mental Retardation Facial Dysmorphism, Hypertrichosis, Epilepsy, Intellectual/Developmental Delay, and Gingival Overgrowth Syndrome facial[rgd.mcw.edu] […] absence of the sternocleidomastoid muscle Congenital adrenal hyperplasia Congenital alopecia X-linked Congenital amegakaryocytic thrombocytopenia Congenital amputation Congenital[personalizedcause.com] syndrome / Welander distal myopathy, Swedish type / Wells-Jankovic syndrome / Werner's syndrome / West syndrome / Weyers acrofacial dysostosis / Weyers ulnar ray/oligodactyly[gennome.com]

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