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10 Possible Causes for Basal Cell Carcinoma, 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] First degree relative with NBCCS Minor criteria Childhood medulloblastoma (also called primitive neuro-ectodermal tumor [PNET]) Lympho-mesenteric or pleural cysts Macrocephaly[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] Absolute or relative macrocephaly has been seen in children and adults with Legius syndrome.[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] Absolute or relative macrocephaly has been seen in children and adults with Legius syndrome.[web.archive.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] Absolute or relative macrocephaly has been seen in children and adults with Legius syndrome.[web.archive.org]

  • 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] Clinical manifestations in 105 persons with nevoid basal cell carcinoma syndrome.[link.springer.com]

  • Fitzsimmons-Guilbert Syndrome

    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] Relative macrocephaly is present during early childhood but head circumference is markedly low by adulthood. Psychomotor development is normal.[nectarmutation.org] cell carcinoma syndrome Infantile axonal neuropathy Ulnar-mammary syndrome Anophthalmia plus syndrome Parkes Weber syndrome X-linked susceptibility to autism-4 Cryptomicrotia[checkrare.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] cell carcinoma syndrome is a syndrome with wide variety of manifestations ranging from oral lesions to skeletal deformities.[biomedsearch.com]

  • 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] carcinoma syndrome ) BMPR1A ( BMPR1A juvenile polyposis syndrome ) IL2RG ( X-linked severe combined immunodeficiency ) See also cell surface receptors[en.wikipedia.org]

  • Stevenson Carey Syndrome

    cell carcinoma syndrome NF1 Microduplication Syndrome Nguyen Syndrome Nicolaides Baraitser Syndrome Nicolau Syndrome Nievergelt Syndrome Nijmegen breakage syndrome Nisch[rgd.mcw.edu] 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 Nicolaides Baraitser Syndrome Nijmegen breakage syndrome Nijmegen Breakage Syndrome-Like Disorder Noble Bass Sherman[rgd.mcw.edu]

  • 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] Expression of Drebrin, an actin binding protein, in basal cell carcinoma, trichoblastoma and trichoepithelioma. Histol Histopathol., 2014; 29: 757-766.[med.nagoya-u.ac.jp]

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