Create issue ticket

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

  • Gorlin Syndrome

    The triad of microtia, absent/hypoplastic patellae, and short stature was observed in 82% of individuals with MGS.[ncbi.nlm.nih.gov] […] 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]

  • Legius Syndrome

    Other less common manifestations include short stature, macrocephaly, Noonan-like facies, pectus excavatum/carinatum, lipomas, hypopigmented macules, vascular lesions, learning[orpha.net] 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]

  • Neurofibromatosis Type 1

    Osteopenia, osteoporosis, bone overgrowth, short stature, macrocephaly, scoliosis, skeletal dysplasia (sphenoid wing, vertebral), and pseudoarthrosis may be present.[web.archive.org] 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]

  • Zori-Stalker-Williams Syndrome

    Zori Stalker Williams Syndrome “Zori Stalker Williams Syndrome” In our body, the developmental bone dis-order, Zori Stalker Williams Syndrome is a familial short stature,[wellnessadvocate.com] Clinical manifestations in 105 persons with nevoid basal cell carcinoma syndrome.[link.springer.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]

  • Neurofibromatosis Type 2

    Additional signs and symptoms of neurofibromatosis type 1 include high blood pressure (hypertension), short stature, an unusually large head (macrocephaly), and skeletal abnormalities[web.archive.org] 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]

  • Fitzsimmons-Guilbert Syndrome

    […] retarded growth, walking difficulty, muscle weakness, webbed fingers, short stature and protruding chest.[besttreatmenthq.com] 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]

  • Opitz-Kaveggia Syndrome

    short stature ( Q77.4 ) hypochondroplastic short stature ( Q77.4 ) nutritional short stature ( E45 ) pituitary short stature ( E23.0 ) progeria ( E34.8 ) renal short stature[icd10data.com] 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]

  • Stevenson Carey Syndrome

    […] and Facial Dysmorphism Mental Retardation, Short Stature, Facial Anomalies, and Joint Dislocations Mental Retardation, Skeletal Dysplasia, and Abducens Palsy Mental Retardation[rgd.mcw.edu] 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]

  • Pseudohypoparathyroidism Type 1B

    Five of 16 subjects had subclinical hypothyroidism; no subject showed sc ossification or short stature.[ncbi.nlm.nih.gov] : 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]

  • Nasopalpebral Lipoma - Coloboma - Telecanthus Syndrome

    […] acheiropody achondrogenesis achondroplasia acrocapitofemoral dysplasia acrodysostosis Acrodysplasia Scoliosis Acrodysplasia with Ossification Abnormalities, Short Stature,[rgd.mcw.edu] 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]

Similar symptoms