Create issue ticket

74 Possible Causes for Congenital Alopecia, Facial Hemiatrophy, Sjögren-Larsson Syndrome

  • Cerebellotrigeminal Dermal Dysplasia

    ) -- Child Syndrome -- Chondrodysplasia Punctata (Cdp) Conradi-Hunermann-Happle Type (Cdpx2) -- SjÖgren-Larsson Syndrome -- Kid Syndrome (Keratitis-Ichthyosis-Deafness) --[library.jkuat.ac.ke] 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]

  • Tollner-Horst-Manzke Syndrome

    syndrome Sjogren-Larsson-like Syndrome Sjögren-Mikulicz Syndrome Skeletal Defects, Genital Hypoplasia, And Mental Retardation Sketetal Dysplasia Coarse Facies Mental Retardation[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] Abnormalities, Kyphoscoliosis, and Mental Retardation Facial Dysmorphism, Hypertrichosis, Epilepsy, Intellectual/Developmental Delay, and Gingival Overgrowth Syndrome facial[rgd.mcw.edu]

  • Lamellar Ichthyosis

    […] of this substrate by the fatty alcohol:nicotinamide-adenine dinucleotide oxidoreductase (FAO) enzyme complex, in which one component, ALDH3A2, is known to be mutated in Sjögren-Larsson[ncbi.nlm.nih.gov] 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]

  • Salti-Salem Syndrome

    syndrome Sjögren's syndrome Skandaitis Skeletal dysplasia brachydactyly Skeletal dysplasia epilepsy short stature Skeletal dysplasia orofacial anomalies Skeletal dysplasia[en.wikipedia.org] 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]

  • Phakomatosis Pigmentokeratotica

    ) Neurocutaneous Melanosis Polyostotic Fibrosis Dysplasia (McCune-Albright syndrome) Sjögren-Larsson syndrome Wyburn-Mason Syndrome Questions for Further Discussion 1.[pediatriceducation.org] 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]

  • Schwartz-Lelek Syndrome

    Larsson syndrome Sjögren's syndrome Skeletal dysplasia brachydactyly Skeletal dysplasia epilepsy short stature Skeletal dysplasia orofacial anomalies Skeletal dysplasia San[wikidoc.org] hemiatrophy Facio Thoraco Genital Syndrome Faciocardiomelic Syndrome Faciocardiorenal Syndrome factitious disorder Failed Back Surgery Syndrome Familial Antiphospholipid[rgd.mcw.edu] ALOPECIA 1[panelapp.genomicsengland.co.uk]

  • Odonto-Onycho-Dermal Dysplasia

    syndrome: see Sjögren-Larsson , syndrome of 5) Keratitis Ichtyosis Deafness (KID) syndrome: see KID syndrome 6) Ichtyosis follicularis alopecia and photophobia (IFAP) syndrome[sites.uclouvain.be] hemiatrophy Oral manifestations of systemic disease[en.wikipedia.org] […] recessive palmoplantar keratoderma and congenital alopecia Bartsocas-Papas syndrome Basal epidermolysis bullosa simplex Benign cephalic histiocytosis Blepharo-cheilo-odontic[se-atlas.de]

  • CANOMAD Syndrome

    syndrome Sjogren-Larsson-like Syndrome Sjögren-Mikulicz Syndrome Skeletal Defects, Genital Hypoplasia, And Mental Retardation Sketetal Dysplasia Coarse Facies Mental Retardation[rgd.mcw.edu] hemiatrophy En coup de sabre Systemic sclerosis (Scleroderma): Subtypes Diffuse cutaneous scleroderma Rapidly progressive Widespread skin thickening Similar syndromes 2 toxins[neuromuscular.wustl.edu] […] absence adrenal alopecia amegakaryocytic aneurysms great antithrombin aplastic arteriovenous shuntCongenital benign spinal muscular atrophy bilateral bronchobiliary cardiovascular[shecandothat.net]

  • Chudley-Rozdilsky Syndrome

    syndrome Sjogren-Larsson-like Syndrome Sjögren-Mikulicz Syndrome Skeletal Defects, Genital Hypoplasia, And Mental Retardation Sketetal Dysplasia Coarse Facies Mental Retardation[rgd.mcw.edu] […] absence of the sternocleidomastoid muscle Congenital adrenal hyperplasia Congenital alopecia X-linked Congenital amegakaryocytic thrombocytopenia Congenital amputation Congenital[personalizedcause.com] congenital alopecia - See Thumb deformity, alopecia, pigmentation anomaly Congenital diaphragmatic defect - See Congenital diaphragmatic hernia Congenital diaphragmatic hernia[elbiruniblogspotcom.blogspot.com]

  • Hallermann-Streiff Syndrome

    syndrome Sjogren-Larsson syndrome Sjogren-Larsson-like Syndrome Sjögren-Mikulicz Syndrome Skin Fragility-Woolly Hair Syndrome Skraban-Deardorff Syndrome Slavotinek Pike Mills[rgd.mcw.edu] Synonym: congenital sutural alopecia, hallermann-streiff syndrome, hallermann-streiff-francois syndrome, mandibulo-oculofacial syndrome, oculomandibulodyscephaly, oculomandibulofacial[biology-online.org] Alopecia 2 Palmoplantar Keratoderma and Congenital Alopecia, Autosomal Dominant Papillon-Lefevre Syndrome Pili Torti and Developmental Delay Pilodental Dysplasia with Refractive[nfed.org]

Similar symptoms