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98 Possible Causes for Congenital Alopecia, Dermatitis, Facial Hemiatrophy

  • 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] […] syndrome大動脈炎症候群 apheresisアフェレーシス aphthaアフタ arthritis関節炎 articular contracture関節拘縮 articular rigidity関節硬直 aseptic necrosis無菌壊死 asthmatic attack喘息発作 atopic asthmaアトピー型喘息 atopic dermatitis[tokyo-med.ac.jp]

  • 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] Holocarboxylase synthetase deficiency, a biotin-responsive multiple carboxylase deficiency (MCD), is characterized by metabolic acidosis, lethargy, hypotonia, convulsions, and dermatitis[mendelian.co]

  • 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] A patient presented with significant vulvar skin atrophy following prolonged steroid application to treat vulvar dermatitis.[ncbi.nlm.nih.gov]

  • 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] Abstract A 78-year-old woman had ectropion of both lower eyelids 4 weeks after the appearance of dermatitis around the eyes.[ncbi.nlm.nih.gov]

  • Linear Atrophoderma of Moulin

    Clinical and serological characteristics of progressive facial hemiatrophy: a case series of 12 patients. J Am Acad Dermatol. Feb 2006;54(2):227-33.[wikidoc.org] The Journal of dermatology 41 (9), 830-833 , 2014 9 2014 Congenital temporal triangular alopecia: A typical Brauer nevus.[scholar.google.com.tr] Abstract Linear atrophoderma, first described by Moulin, is an acquired unilateral dermatitis localized along the Blaschko lines.[ncbi.nlm.nih.gov]

  • Trachonychia

    hemiatrophy – Boggy, crusted, pustules – Suppuration, PMNs and eosinophils – AKA perifolliculitis capitis abscedens et suffodiens – Black males – Inflammation, bogginess[brainscape.com] Scarring hair loss, also known as cicatricial alopecia, is the loss of hair which is accompanied with scarring.[studylib.net] It has also been associated with other diseases such as eczema , psoriasis, alopecia areata, and atopic dermatitis. [2] Trachonychia is often seen in vitiligo patients – suggesting[medbox.iiab.me]

  • Peeling Skin Syndrome Type A

    hemiatrophy Facio Thoraco Genital Syndrome Faciocardiomelic Syndrome Faciocardiorenal Syndrome factitious disorder Failed Back Surgery Syndrome Familial Antiphospholipid[rgd.mcw.edu] , lamellar type 4 LIPN Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis CLDN1 Ichthyosis, spastic quadriplegia, and mental retardation ELOVL4 Ichthyosis[centogene.com] […] epidermolytic ichthyosis, autosomal recessive congenital ichthyosis, staphylococcal scalded skin syndrome, Netherton syndrome, pemphigus foliaceus (see these terms), atopic dermatitis[orpha.net]

  • Amelo-Onycho-Hypohidrotic Syndrome

    hemiatrophy Facio Thoraco Genital Syndrome Faciocardiomelic Syndrome Faciocardiorenal Syndrome factitious disorder Failed Back Surgery Syndrome Familial Antiphospholipid[rgd.mcw.edu] alopecia [ ] Autosomal dominant periodic fever [ ] Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis [ ] Autosomal dominant popliteal pterygium[wikicure.fandom.com] […] frequent (99-80%) 18 marked delay in eruption of permanent teeth 33 HP:0006291 Symptoms via clinical synopsis from OMIM: 58 Skin Nails Hair Skin: hypohidrosis seborrheic dermatitis[malacards.org]

  • 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] It has been shown that patients suffering from atopic dermatitis have a reduced ceramide content in the stratum corneum, whereas in the stratum corneum of lamellar ichthyosis[ncbi.nlm.nih.gov]

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