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3,839 Possible Causes for Epidermolysis Bullosa, Fetal Disorder, Syndactyly Does Not Occur

  • Adhesion of Amnion to Fetus

    Intrapartum Assessment of Fetal Health, Pathogenesis of Pre-term Birth, Maternal and Fetal Infectious Disorders, and Benign Gynecological Conditions of Pregnancy.[books.google.com] The cutaneious syndactyly seen usually does not involve underlying bony fusion. A strong relationship between ABS and clubfoot exists.[podiatrynetwork.com] In rare situations, it may be associated with: Ehlers-Danlos syndrome epidermolysis bullosa There is a massive spectrum of abnormalities, depending on which part becomes entrapped[radiopaedia.org]

  • Herlitz Disease

    What is Herlitz Junctional Epidermolysis Bullosa, LAMB3-related?[counsyl.com] Martin Carter Springer Science & Business Media , ٠٦‏/١٢‏/٢٠١٢ - 302 من الصفحات Because skin blisters are the initial manifestation of epidermolysis bullosa (EB), patients[books.google.com] These findings supported a diagnosis of junctional epidermolysis bullosa. The patient was treated with topical and systemic antibiotics.[ncbi.nlm.nih.gov]

    Missing: Fetal Disorder
  • Cenani Syndactylism

    DDG2P Version 1.8 review BIALLELIC, autosomal or pseudoautosomal Sources DD-Gene2Phenotype Expert Review Green Phenotypes CENANI-LENZ SYNDACTYLY SYNDROME 212780 LRP4 in Fetal[panelapp.genomicsengland.co.uk] In some fetuses, this process does not occur completely between all fingers or toes and some residual webbing remains.[en.academic.ru] bullosa with pyloric atresia EDAR ( EDAR Hypohidrotic ectodermal dysplasia ) · PTCH1 ( Nevoid basal cell carcinoma syndrome ) · BMPR1A ( BMPR1A Juvenile polyposis syndrome[dictionary.sensagent.com]

  • Congenital Malformation

    Most techniques requiring samples of fetal material for analysis carry some degree of risk to the pregnancy.[ncbi.nlm.nih.gov] ICD-10-CM Range Q80-Q89 Other congenital malformations Q80 Congenital ichthyosis Q81 Epidermolysis bullosa Q82 Other congenital malformations of skin Q83 Congenital malformations[icd10data.com] Alcohol consumption and certain drugs during pregnancy significantly increase the risk that a baby will be born with abnormalities (e.g. fetal alcohol spectrum disorders )[healthychildren.org]

    Missing: Syndactyly Does Not Occur
  • Fetus Papyraceous

    Stay on top of rapidly evolving maternal-fetal medicine through new chapters on Recurrent Spontaneous Abortion, Stillbirth, Patient Safety, Maternal Mortality, and Substance[books.google.de] Epidermolysis Bullosa Research Association of Australia (DebRA) to rapidly diagnose and manage these patients.[racgp.org.au] Hence, CT disorders such as EDS possibly alter the fetal membranes inducing PPROM and miscarriages.[hoajonline.com]

    Missing: Syndactyly Does Not Occur
  • Congenital Muscular Dystrophy

    Suggestive of a prenatal origin of the hypotonia in infancy are the following: family history (consanguineity, familial muscle disorder); pregnancy history (reduced fetal[doi.org] Abstract Mutations in the PLEC1 gene encoding plectin have been reported in neonatal epidermolysis bullosa simplex with muscular dystrophy of later-onset (EBS-MD).[ncbi.nlm.nih.gov] Patients CMD with familial junctional epidermolysis bullosa often have brain atrophy and enlarged ventricles on MRI.[emedicine.medscape.com]

    Missing: Syndactyly Does Not Occur
  • Amniotic Band Syndrome

    Amniotic band syndrome is a rare congenital disorder caused by entrapment of fetal parts by fibrous amniotic bands in utero.[ncbi.nlm.nih.gov] The cutaneious syndactyly seen usually does not involve underlying bony fusion. A strong relationship between ABS and clubfoot exists.[podiatrynetwork.com] We describe two male infants born with features of dystrophic epidermolysis bullosa (DEB) and ABS.[ncbi.nlm.nih.gov]

  • Robinow Syndrome

    Robinow (fetal face) syndrome is a rare inherited multisystem disorder featuring mesomelic or acromesomelic limb shortening, facial and spinal deformities, hypoplastic genitalia[ncbi.nlm.nih.gov] Partial cutaneous syndactyly occurs in the hands and feet, but does not produce a consistent pattern.[jmg.bmjjournals.com] bullosa with pyloric atresia EDAR ( EDAR hypohidrotic ectodermal dysplasia ) PTCH1 ( Nevoid basal-cell carcinoma syndrome ) BMPR1A ( BMPR1A juvenile polyposis syndrome )[en.wikipedia.org]

  • Epidermolysis Bullosa Simplex

    Epidermolysis bullosa simplex (Koebner) is a keratin disorder. Ultrastructural and immunohistochemical study. Arch. Dermatol. 127 :367-372.[dx.doi.org] Epidermolysis bullosa simplex is one of a group of genetic conditions called epidermolysis bullosa that cause the skin to be very fragile and to blister easily.[ghr.nlm.nih.gov] […] encoding keratin 5 or keratin 14 Epidermolysis bullosa simplex (disorder) Epidermolysis bullosa simplex Weber–Cockayne syndrome Statements Epidermolysis bullosa simplex Identifiers[wikidata.org]

    Missing: Syndactyly Does Not Occur
  • Amniotic Band

    Amniotic band syndrome is a rare congenital disorder caused by entrapment of fetal parts by fibrous amniotic bands in utero.[ncbi.nlm.nih.gov] The cutaneious syndactyly seen usually does not involve underlying bony fusion. A strong relationship between ABS and clubfoot exists.[podiatrynetwork.com] In rare situations, it may be associated with: Ehlers-Danlos syndrome epidermolysis bullosa There is a massive spectrum of abnormalities, depending on which part becomes entrapped[radiopaedia.org]

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