Create issue ticket

10 Possible Causes for Basal Cell Carcinoma, Hypertelorism, Relative Macrocephaly in Childhood

  • Gorlin Syndrome

    […] syndrome (disorder) Naevoid basal cell carcinoma syndrome basal cell nevus syndrome Gorlin syndrome edit English nevoid basal cell carcinoma syndrome an autosomal dominant[wikidata.org] […] with NBCCS childhood medulloblastoma macrocephaly (occipital frontal circumference 97th centile) cleft lip/palate vertebral/rib anomalies preaxial or postaxial polydactyly[invitae.com] Because of macrocrania, hypertelorism and epidermal punctiform lesions in the palm of the hand, Gorlin syndrome was clinically suspected and molecularly confirmed by finding[ncbi.nlm.nih.gov]

  • Neurofibromatosis Type 1

    Gorlin Syndrome (nevoid basal cell carcinoma syndrome) Risk of developing cancerous and noncancerous tumors, most often basal cell carcinoma, less often meduloblastoma during[doi.org] The number of café au lait macules increases with age in childhood, similar to what is observed in NF1 [Author, personal observation]. Macrocephaly.[web.archive.org] […] frequent than in NF1) Multiple café-au-lait spots (an autosomal dominant trait without other features of neurofibromatosis) LEOPARD syndrome (multiple lentigines, ocular hypertelorism[en.wikibooks.org]

  • Legius Syndrome

    Gorlin Syndrome (nevoid basal cell carcinoma syndrome) Risk of developing cancerous and noncancerous tumors, most often basal cell carcinoma, less often meduloblastoma during[scielo.br] The number of café au lait macules increases with age in childhood, similar to what is observed in NF1 [Author, personal observation]. Macrocephaly.[ncbi.nlm.nih.gov] Individuals with Legius syndrome typically have multiple cafe-au-lait spots, sometimes associated with skin fold freckling, variable dysmorphic features such as hypertelorism[diseaseinfosearch.org]

  • Opitz-Kaveggia Syndrome

    cell carcinoma syndrome, Basal Cell Nevus Syndrome, Gorlin syndrome 20301330 PTEN Cowden syndrome, Bannayan-Riley-Ruvalcaba syndrome (BRRS) PTEN related hamartoma syndrome[web.labmed.washington.edu] The key elements of the clinical phenotype are absolute or relative macrocephaly with a long narrow face; tall forehead; dolicocephalic head shape; an open mouth; small, simple[nature.com] Opitz-Frias syndrome Micrognathia and a broad and flat nasal bridge with marked hypertelorism in a neonate with Opitz-Frias syndrome.[accessanesthesiology.mhmedical.com]

  • Nasopalpebral Lipoma - Coloboma - Telecanthus Syndrome

    Basal cell carcinoma B. Capillary hemangioma C. Conjunctiva amyloidosis 3. Medications A. Epinephrine B. Idoxuridine C. Phospholine iodide D. Pilocarpine E. Practolol F.[dentisty.org] ., 2017 Patient 4 Japanese case F M General characteristics Gender M Country of origin M F China M Germany Japan Clinical features Short stature Relative macrocephaly at birth[docksci.com] 6011000124106 MAPTARGET H90.5 6011000124106 MAPPRIORITY 1 6011000124106 MAPRULE OTHERWISE TRUE 6011000124106 MAPRULE IFA 724280001 Hypospadias, hypertelorism, coloboma, deafness[bioportal.bioontology.org]

  • Neurofibromatosis Type 2

    Although this is usually of cosmetic significance only, melanoma and basal cell carcinoma have been reported in adults with NF1; however, the risk for developing these malignancies[pediatrics.aappublications.org] The number of café au lait macules increases with age in childhood, similar to what is observed in NF1 [Author, personal observation]. Macrocephaly.[web.archive.org] Synopsis cephalic anomalies macrocephaly sphenoid dysplasia Lisch nodules (iris hamartomas) glaucoma hypertelorism vascular anomalies renal artery stenosis skeletal anomalies[humpath.com]

  • Stevenson Carey Syndrome

    The number of café au lait macules increases with age in childhood, similar to what is observed in NF1 [Author, personal observation]. Macrocephaly.[ncbi.nlm.nih.gov] cell carcinoma syndrome NF1 Microduplication Syndrome Nguyen Syndrome Nicolaides Baraitser Syndrome Nicolau Syndrome Nievergelt Syndrome Nijmegen breakage syndrome Nisch[rgd.mcw.edu] Facies is characterized by, hypertelorism, big and large nose, micrognathia and others craniofacial abnormalities 1,2 .[scielo.iec.gov.br]

  • Fitzsimmons-Guilbert Syndrome

    Relative macrocephaly is present during early childhood but head circumference is markedly low by adulthood. Psychomotor development is normal.[nectarmutation.org] CELL NEVUS SYNDROME NEVOID BASAL CELL CARCINOMA (BCC) SYNDROME GORLIN-GOLTZ SYNDROME syndrome of autosomal dominant inheritance characterized by (1) multiple cutaneous basal[radiologykey.com] It may or may not be associated with hypertelorism.[entokey.com]

  • Zori-Stalker-Williams Syndrome

    Cell Carcinoma Bed Baths, Ayurveda Treatment For Bedwetting, Ayurveda Treatment For Benzodiazepine Abuse, Ayurveda Treatment For Bicycle Helmets Bicycle Safety, Ayurveda[ayurdoctor.com] […] nails syndrome is a rare multiple congenital anomalies syndrome characterized by relative macrocephaly, pectus excavatum, short stature, nail dysplasia, and motor developmental[orpha.net] , microtia, facial clefting syndrome Hypertelorism, Severe, with Midface Prominence, Myopia, Mental Retardation, and Bone Fragility Hypertrichosis, Hyperkeratosis, Mental[rgd.mcw.edu]

  • Pseudohypoparathyroidism Type 1B

    : AGM3, 6 Integrin : LAD1 Glanzmann's thrombasthenia Junctional epidermolysis bullosa with pyloric atresia EDAR ( EDAR hypohidrotic ectodermal dysplasia ) PTCH1 ( Nevoid basal-cell[en.wikipedia.org] Many patients have relatively high birth weight and/or early-onset obesity that persists into childhood and later; relative macrocephaly and tall stature have also been observed[academic.oup.com] […] recurrent pancreatitis with calcification and duct stones, learning difficulties and some features of Albright’s Hereditary Osteodystrophy (AHO) including round facies, hypertelorism[esa-srb-anzbms-2016.p.asnevents.com.au]

Similar symptoms