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13 Possible Causes for Epidermolysis Bullosa, Lymphedema, Syndactyly Does Not Occur

  • Herlitz Disease

    […] syndrome,607823 SOX1827.10.830.59Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome,137940 SOX2111.40.990.97Microphthalmia, syndromic 3206900 SOX2111.40.990.97Optic[qgenomics.com] What is Herlitz Junctional Epidermolysis Bullosa, LAMB3-related?[counsyl.com] […] type VI 604320 IKBKAP 9q31.3 Dysautonomia, familial 223900 IKBKG Xq28 Ectodermal dysplasia, hypohidrotic, with immune deficiency 300291 Ectodermal, dysplasia, anhidrotic, lymphedema[institutobernabeu.com]

  • Amniotic Band

    Follow-up over a 6-year period enables us to provide a favorable outlook with regard to functional use of the extremity and absence of chronic lymphedema, but she does have[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]

  • Amniotic Band Syndrome

    […] extremity limb malformations are extremely common and consist of asymmetric digital ring constrictions, distal atrophy, congenital intrauterine amputations, acrosyndactyly, lymphedema[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]

  • Intestinal Pseudo-Obstruction - Patent Ductus Arteriosus - Natal Teeth

    […] syndrome H02168 Hypotrichosis-lymphedema-telangiectasia syndrome H02220 MEDNIK syndrome [PATH: hsa04142 ] H02295 Adermatoglyphia [PATH: hsa04550 ] H02296 Basan syndrome [[genome.jp] Postaxial polydactyly of the feet does occur, as does (partial) syndactyly of the second and third toes or third and fourth fingers.[docplayer.net] Epidermolysis bullosa simplex: review and report of case. ASDC J Dent Child, 1998; 65(5):349-353. 70. Liu M, Huang W. Oral abnormalities in Taiwanese newborns.[vdocuments.mx]

  • Cenani Syndactylism

    Short -rib thoracic dysplasia with or without polydactyly IHH Acrocapitofemoral dysplasia, Brachydactyly, Syndactyly type Lueken IKBKG Ectodermal, dysplasia, anhidrotic, lymphedema[genda.com.ar] 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]

  • Adhesion of Amnion to Fetus

    Deep circumferential constriction band of right lower limb extremity associated with marked lymphedema and right clubfoot.[ispub.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]

  • Congenital Absence of Both Lower Leg and Foot

    Early surgical intervention is necessary to prevent progressive lymphedema.[ahni.com] […] simplex Q811Epidermolysis bullosa letalis Q812Epidermolysis bullosa dystrophica Q818Other epidermolysis bullosa Q819Epidermolysis bullosa, unspecified Q820Hereditary lymphedema[cms.gov] bullosa Keratoderma (congenital) Excludes: pilonidal cyst (685.0-685.1) 757.4 Specified anomalies of hair Congenital: alopecia atrichosis beaded hair hypertrichosis monilethrix[theodora.com]

  • Brachydactyly Coloboma and Anterior Segment Dysgenesis

    […] regulatory protein defects Other well-defined immunodeficiency syndromes Autoimmune lymphoproliferative syndromes Familial hemophagocyic lymphohistiocytosis Osteoporosis, lymphedema[csirnotes.com] When cryptophthalmos occurs in association with other systemic abnormalities, as it often does, the condition is described as cryptophthalmos syndrome.[entokey.com] bullosa dystrophica, AD ZFLNCG06123 601088 Ayme-Gripp syndrome ZFLNCG11173 613310 Exudative vitreoretinopathy 5 ZFLNCG02289 611664 Skin/hair/eye pigmentation 7, blond/brown[zflnc.org]

  • Syndactyly

    […] for vascular compromise treatment may be for cosmetic purposes can wait until child is older staged hemi-circumferential z-plasty technique deep bands with distal edema/lymphedema[brainscape.com] This condition does not have a notable cause and may occur in isolation or is inherited.[epainassist.com] Secondary syndactyly, also called "pseudosyndactyly", is rare and can be a complication of burns, dystrophic epidermolysis bullosa or trauma.[ncbi.nlm.nih.gov]

  • Apert Syndrome

    The findings are dwarfism, webbed neck, low hairline, epicanthal folds, mandibular deformity, webbed elbows and knees, coarctation of the aorta, hypertension, lymphedema of[emedicine.medscape.com] Unlike Apert syndrome, however, PS does not generally cause syndactyly of the hands.[forgottendiseases.org] bullosa with pyloric atresia EDAR ( EDAR hypohidrotic ectodermal dysplasia ) PTCH1 ( Nevoid basal-cell carcinoma syndrome ) BMPR1A ( BMPR1A juvenile polyposis syndrome )[en.wikipedia.org]

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