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4,191 Possible Causes for Alopecia, Focal Keratoderma of Soles, Maxillary Hypoplasia

  • Growth Hormone Deficiency

    Palmoplantar keratoderma (PPK) is a diverse group of disorders, characterized by thickening of the palms and soles, which are subdivided into focal or diffuse; it can be acquired[] In children suffering from significant GH deficiency the facial features are distinguished by a prominence of the forehead and maxillary hypoplasia.[] The non-inflammatory type usually will not be complicated by scarring alopecia.[]

  • Rapp-Hodgkin Syndrome

    Abstract An 8-year-old girl with narrow nose, small mouth, maxillary hypoplasia, cleft palate, hypodontia and hypohidrosis is described.[] The ectodermal dysplasia manifests through uncombable, sparse, wiry hair; alopecia in adulthood; hypodontia; hypohidrosis; and dysplastic nails.[] Università degli Studi - Torino, Dipartimento di Discipline Medico-Chirurgiche, Sezione Dermatologia PDF A 23-year old woman with narrow nose, maxillary hypoplasia, cleft[]

    Missing: Focal Keratoderma of Soles
  • Tricho-Retino-Dento-Digital Syndrome

    Alopecia antibody deficiency Alopecia totalis Alopecia universalis Alopecia-contractures-dwarfism-intellectual disability syndrome Alopecia-epilepsy-pyorrhea-intellectual[] […] cell immunodeficiency primary TRAPS (TNF-receptor-associated periodic syndrome) Taurodontia absent teeth sparse hair Teebi Naguib Alawadi syndrome Teeth noneruption of with maxillary[] hypoplasia and genu valgum Tel Hashomer camptodactyly syndrome Telangiectasia ataxia variant V1 Telangiectasia, hereditary hemorrhagic Telangiectasia Telecanthus hypertelorism[]

    Missing: Focal Keratoderma of Soles
  • Spondyloepimetaphyseal Dysplasia-Hypotrichosis Syndrome

    Hypoplasia and Brachydactyly Metaphyseal Dysplasia with Maxillary Hypoplasia with or without Brachydactyly Metaphyseal Dysplasia without Hypotrichosis Metaphyseal Dysplasia[] Congenital malformation H00740 Ichthyosis follicularis, alopecia, and photophobia syndrome Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome is a rare X-linked[] , Metaphyseal dysplasia without hypotrichosis RUNX2 Cleidocranial dysplasia, Metaphyseal dysplasia with maxillary hypoplasia SBDS Aplastic anemia, Severe spondylometaphyseal[]

    Missing: Focal Keratoderma of Soles
  • Chondrodysplasia Punctata

    It is an X-linked recessive disorder and is characterized by a flat nasal tip, short columella and maxillary hypoplasia, involvement of terminal phalanges, and stippled chondrodystrophy[] A 5-year-old girl presented for evaluation of ill-defined patches of cicatricial alopecia.[] Severe maxillary hypoplasia or maxillary retrognathia may require reconstructive surgery in older individuals.[]

    Missing: Focal Keratoderma of Soles
  • Metaphyseal Acroscyphodysplasia

    The association of metaphyseal acroscyphodysplasia with psychomotor delay and alopecia has also been reported in some cases.Visit the Orphanet disease page for more resources[] 1 A three-generation family with metaphyseal dysplasia, maxillary hypoplasia and brachydactyly (MDMHB) due to intragenic RUNX2 duplication. ( 29891876 ) 2018 2 Resolution[] The association of metaphyseal acroscyphodysplasia with psychomotor delay and alopecia has also been reported in some cases.[]

    Missing: Focal Keratoderma of Soles
  • Thoracomelic Dysplasia

    -2-hydroxyglutaric aciduria Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome Metaphyseal dysplasia, Braun-Tinschert type Metaphyseal dysplasia-maxillary[] […] malformations Osteochondritis of tarsal bone Osteochondrosis of the tibial Thoracic outlet syndrome Benign familial hematuria EB-PA Johnson neuroectodermal syndrome tubercle TOS Alopecia[] Hypoplasia and Genu Valgum OMIM:187000 Teeth, Odd Shapes of OMIM:187050 Teeth Present at Birth OMIM:187100 Teeth, Supernumerary OMIM:187260 Telangiectasia, Hereditary Benign[]

    Missing: Focal Keratoderma of Soles
  • Acroosteolysis-Keloid-Like Lesions-Premature Aging Syndrome

    Zygomatic arch hypoplasia Delayed closure of fontanels Maxillary hypoplasia Thin calvarium - Osteopenia - Delayed bone maturation Spine Scoliosis (in some patients) Hands[] Alopecia of the scalp, eyebrows, and eyelashes, aswell as prominent scalp veins were evident.[] hypoplasia and genu valgum Mosaic trisomy 14 Charcot-Marie-Tooth disease Charcot-Marie-Tooth disease Dystelephalangy Microphthalmia syndromic 8 Acheiropody Short stature[]

    Missing: Focal Keratoderma of Soles
  • Diffuse Palmoplantar Keratoderma

    […] involving the whole of the palms and soles. [1] : 506-8 [2] : 213 Focal Focal palmoplantar keratoderma, a type of palmoplantar keratoderma in which large, compact masses[] The hair is sparse and pale, and the alopecia can be patchy or total. Hair loss may lead to total alopecia by puberty.[] Alopecia, deafness, nail dystrophy, and dental loss may be associated.[]

    Missing: Maxillary Hypoplasia
  • Salti-Salem Syndrome

    hypoplasia-brachydacty syndrome Microcephaly Cervical Spine Fusion Anomalies Microcephaly Deafness Syndrome Microcephaly Sparse Hair Mental Retardation Seizures Microcephaly[] Patients present with fine, scanty hair and frontoparietal alopecia.[] Name Alopecia Synonyms AGA1 Alopecia, Androgenetic ALOPECIA, ANDROGENETIC, 1 Alopecia, Androgenic Alopecia Cicatrisata Alopecia Cicatrisatas Alopecia, Male Pattern Alopecias[]

    Missing: Focal Keratoderma of Soles

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