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17 Possible Causes for Androgenic Alopecia, Congenital Alopecia, Facial Hemiatrophy

  • 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] , Androgenic Androgenetic Alopecia ANDROGENETIC ALOPECIA;AGA BALDNESS, MALE PATTERN, INCLUDED Androgenic Alopecia Androgenic Alopecias Baldness Baldness, Female Pattern Baldness[ctdbase.org]

  • Auriculocondylar Syndrome

    hemiatrophy Oral manifestations of systemic disease[en.wikipedia.org] […] androgenic alopecia , see androgenetic alopecia ANE1 , see acute necrotizing encephalopathy type 1 Anemia, Dyserythropoietic, Congenital , see congenital dyserythropoietic[herenciageneticayenfermedad.blogspot.com] Melkersson–Rosenthal syndrome Microstomia Noma Oral Crohn's disease Orofacial granulomatosis Perioral dermatitis Pyostomatitis vegetans Other Eagle syndrome Hemifacial hypertrophy Facial[en.wikipedia.org]

  • Autosomal Recessive Spastic Ataxia with Leukoencephalopathy

    543 2 瘢痕回(ulegyria) 544 6 側頭脳瘤(temporal encephalocele) 545 7 Rasmussen脳炎(Rasmussen's encephalitis) 546 8 神経節膠腫(ganglioglioma) 549 9 Parry-Romberg症候群(進行性顔面片側萎縮症progressive facial[rnavi.ndl.go.jp] alopecia Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis Autosomal dominant spastic ataxia Autosomal dominant spastic paraplegia type 4 Autosomal[sanfordresearch.org] […] insensitivity syndrome androgen receptor deficiency, see androgen insensitivity syndrome androgen resistance syndrome, see androgen insensitivity syndrome androgenetic alopecia[mygenomics.com]

  • Autosomal Recessive Spastic Paraplegia Type 28

    543 2 瘢痕回(ulegyria) 544 6 側頭脳瘤(temporal encephalocele) 545 7 Rasmussen脳炎(Rasmussen's encephalitis) 546 8 神経節膠腫(ganglioglioma) 549 9 Parry-Romberg症候群(進行性顔面片側萎縮症progressive facial[rnavi.ndl.go.jp] Genetic Testing - T cell immunodeficiency, congenital alopecia and nail dystrophy (T-cell immunodeficiency, congenital alopecia and nail dystrophy) - Gen FOXN1.[ivami.com] hemiatrophy: PFH) 553 10 Sylvius裂脂肪腫(sylvian fissure lipoma) 555 第16章 神経内科疾患と間違えやすい腫瘍性疾患 1 血管内大細胞型B細胞リンパ腫(intravascular large B-cell lymphoma: IVLBCL) 560 2 リンパ腫様肉芽腫症(lymphomatoid[rnavi.ndl.go.jp]

  • Lamellar Ichthyosis

    Parrot’s lines depressed linear scars radiating from anus, mouth, & nose like wheel spokes; congenital syphilis AKA rhagades Parry-Romberg s. facial hemiatrophy, hyperpigmentation[yumpu.com] Nails: Secondary dystrophy with nail fold inflammation Epidermolytic hyperkeratosis (p. 6) X linked ichthyosis (p. 4) Congenital ichthyosiform erythroderma (p. 12) Netherton[cram.com] Bart's s. 2000, Derm Facts postmenopausal women, excess adrenocortical androgens; diabetes, hirsutism & masculinization Hori's nevus Dunnigan s.[readbag.com]

  • Autosomal Recessive Spastic Paraplegia Type 14

    543 2 瘢痕回(ulegyria) 544 6 側頭脳瘤(temporal encephalocele) 545 7 Rasmussen脳炎(Rasmussen's encephalitis) 546 8 神経節膠腫(ganglioglioma) 549 9 Parry-Romberg症候群(進行性顔面片側萎縮症progressive facial[rnavi.ndl.go.jp] Genetic Testing - T cell immunodeficiency, congenital alopecia and nail dystrophy (T-cell immunodeficiency, congenital alopecia and nail dystrophy) - Gen FOXN1.[ivami.com] , Autosomal Recessive 8 1 Ichthyosis, Congenital, Autosomal Recessive 9 1 Ichthyosis, Congenital, Autosomal Recessive, Nipal4-Related 2 Ichthyosis, Cyclic, With Epidermolytic[preventiongenetics.com]

  • Roifman Syndrome

    Abnormalities, Kyphoscoliosis, and Mental Retardation facial hemiatrophy Facio Thoraco Genital Syndrome Faciocardiomelic Syndrome Faciocardiorenal Syndrome factitious disorder[rgd.mcw.edu] […] dystrophies AGK SengersDNA10 sengers syndrome(cardiomyopathic mitochondrial DNA depletion syndrome-10) NR2E3 S enhanced s cone syndrome FOXN1 T-- t cell immunodeficiency congenital[dokumen.tips] alopecia areata capitis loose anagen planopilaris decalvans keloidalis nuchae Nail onychomycosis paronychia ingrown Mucous membrane Aphthous stomatitis oral leukoplakia cicatricial[add-value.be]

  • Vásquez-Hurst-Sotos Syndrome

    hemiatrophy Facio Thoraco Genital Syndrome Faciocardiomelic Syndrome Faciocardiorenal Syndrome factitious disorder Failed Back Surgery Syndrome Familial Antiphospholipid[rgd.mcw.edu] Infarcts and Leukoencephalopathy Chang Davidson Carlson Syndrome Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism Chudley-Rozdilsky Syndrome Congenital[rgd.mcw.edu] Adrenal Hypoplasia with Precocious Puberty Congenital Alopecia X-Linked Congenital Heart Defects, X-Linked congenital hypogammaglobulinemia Congenital Idiopathic Intestinal[rgd.mcw.edu]

  • Trichodental Syndrome

    Abnormalities, Kyphoscoliosis, and Mental Retardation facial hemiatrophy Facio Thoraco Genital Syndrome Faciocardiomelic Syndrome Faciocardiorenal Syndrome factitious disorder[rgd.mcw.edu] Alopecia 2 Palmoplantar Keratoderma and Congenital Alopecia, Autosomal Dominant Papillon-Lefevre Syndrome Pili Torti and Developmental Delay Pilodental Dysplasia with Refractive[nfed.org] (AADH) syndrome Johnson-McMillin syndrome 147770 Alopecia mental retardation syndrome Perniola syndrome 203650 Alopecia-onchodysplasia-hypohidrosis syndrome Alopecia-onchodysplasia-hypohidrosis-hyperkeratosis-deafness[keratin.com]

  • Rosselli-Gulienetti Syndrome

    Dysmorphism, Cleft Palate, Hearing Loss, and Camptodactyly facial hemiatrophy Facio Thoraco Genital Syndrome Faciocardiomelic Syndrome Faciocardiorenal Syndrome factitious[rgd.mcw.edu] Alopecia 2 Palmoplantar Keratoderma and Congenital Alopecia, Autosomal Dominant Papillon-Lefevre Syndrome Pili Torti and Developmental Delay Pilodental Dysplasia with Refractive[nfed.org] (AADH) syndrome Johnson-McMillin syndrome 147770 Alopecia mental retardation syndrome Perniola syndrome 203650 Alopecia-onchodysplasia-hypohidrosis syndrome Alopecia-onchodysplasia-hypohidrosis-hyperkeratosis-deafness[keratin.com]

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