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Dermatology Online Journal, ISSN 1087-2108, 2018, Volume 24, Issue 1
Precalcaneal congenital fibrolipomatous hamartoma is a benign condition of infancy that is sometimes misdiagnosed due to lack of reports in the literature.... 
Precalcaneal | Fibrolipomatous | Congenital | Dermatology | Pediatric | Hamartoma | Hamartoma - pathology | Heel - diagnostic imaging | Heel - pathology | Hamartoma - diagnostic imaging | Humans | Ultrasonography | Skin - diagnostic imaging | Female | Infant | Heel - abnormalities | Hamartoma - congenital | Skin - pathology
Journal Article
Journal of Cutaneous Pathology, ISSN 0303-6987, 04/2019, Volume 46, Issue 4, pp. 277 - 279
Precalcaneal congenital fibrolipomatous hamartoma (PCFH) is a benign under‐reported condition of infancy characterized by the presence of soft nodules on... 
fibrolipomatous hamartoma | precalcaneal congenital fibrolipomatous hamartoma | congenital piezogenic‐like papules | pedal papules | congenital piezogenic-like papules | PATHOLOGY | DERMATOLOGY | Hamartoma - pathology | Heel - pathology | Humans | Female | Infant | Heel - abnormalities | Hamartoma - congenital | Genetic disorders | Hamartoma | Neoplasia | Skin | Nodules
Journal Article
Best Practice & Research: Clinical Gastroenterology, ISSN 1521-6918, 2010, Volume 24, Issue 5, pp. 573 - 584
Abstract Fibrocystic diseases affecting the liver and often also other organs like the kidneys are a clinically and genetically heterogeneous group of... 
Gastroenterology and Hepatology | PRKCSH | Joubert syndrome | Ciliopathies | Peribiliary cysts | Bardet-Biedl syndrome | PKD2 | PKD1 | PKHD1 | Early and severe disease manifestation | BBS | Autosomal dominant polycystic liver disease (PCLD) | JBTS | von Meyenburg complexes | Congenital hepatic fibrosis | SEC63 | Cilia | Biliary hamartoma | Fibrocystic diseases | Choledochal cysts | Jeune syndrome | Variable disease expression | MKS | Autosomal dominant polycystic kidney disease (ADPKD) | Caroli’s disease | Meckel-Gruber syndrome | Autosomal recessive polycystic kidney disease (ARPKD) | Ductal plate malformation | Caroli's disease | MOLECULAR CHARACTERIZATION | QUALITY-CONTROL | PCLD | SECRETORY PATHWAY | IMAGING EVALUATION | Autosomal dominant polycystic liver disease | INTRAHEPATIC PERIBILIARY GLANDS | BILE-DUCT CYSTS | PKHD1 MUTATIONS | GLUCOSIDASE-II | POLYCYSTIC KIDNEY-DISEASE | SURGICAL-MANAGEMENT | Caroli s disease | GASTROENTEROLOGY & HEPATOLOGY | Liver Diseases - genetics | Humans | Choledochal Cyst - diagnostic imaging | Liver Diseases - diagnostic imaging | Biliary Tract Diseases - diagnosis | Choledochal Cyst - classification | Polycystic Kidney, Autosomal Dominant - genetics | Cysts - diagnostic imaging | Liver Diseases - congenital | Polycystic Kidney, Autosomal Dominant - diagnosis | Liver - diagnostic imaging | Cysts - congenital | Ultrasonography | Polycystic Kidney, Autosomal Dominant - physiopathology | Liver Diseases - physiopathology | Bile Ducts, Intrahepatic - embryology | Hamartoma - diagnosis | Liver diseases | Genetic disorders
Journal Article
Journal Article
Journal of Investigative Dermatology, ISSN 0022-202X, 09/2013, Volume 133, Issue 9, pp. 2229 - 2236
Congenital melanocytic nevi (CMN) can be associated with neurological abnormalities and an increased risk of melanoma. Mutations in , , and have been described... 
MC1R | VARIANTS | RAS | BRAF MUTATIONS | HIGH-FREQUENCY | PHENOTYPE | NEUROLOGICALLY ASYMPTOMATIC CHILDREN | ASSOCIATION | REGISTRY | MOSAICISM | DERMATOLOGY | Meningeal Neoplasms - epidemiology | Prevalence | Nevus, Pigmented - epidemiology | Humans | Child, Preschool | Male | Neurocutaneous Syndromes - congenital | Meningioma - genetics | Mutation, Missense - genetics | Loss of Heterozygosity - genetics | Hamartoma - pathology | Young Adult | Hamartoma - genetics | Nevus, Pigmented - genetics | Meningioma - epidemiology | Zygote | Female | Genetic Predisposition to Disease - epidemiology | Neurocutaneous Syndromes - epidemiology | Child | Melanosis - epidemiology | Melanosis - genetics | Neurocutaneous Syndromes - genetics | Genetic Predisposition to Disease - genetics | Meningeal Neoplasms - genetics | Membrane Proteins - genetics | Central Nervous System Neoplasms - genetics | Risk Factors | Hamartoma - epidemiology | Central Nervous System Neoplasms - epidemiology | Melanosis - congenital | Skin Neoplasms - epidemiology | Nevus, Pigmented - congenital | Magnetic Resonance Imaging | Meningioma - pathology | Central Nervous System Neoplasms - pathology | GTP Phosphohydrolases - genetics | Skin Neoplasms - congenital | Skin Neoplasms - genetics | Adolescent | Mosaicism | Meningeal Neoplasms - pathology | Index Medicus | Original
Journal Article
Journal of Indian Association of Pediatric Surgeons, ISSN 0971-9261, 10/2018, Volume 23, Issue 4, pp. 222 - 224
Congenital nevi and fibrolipomatous hamartoma are benign tumors of childhood, the latter being very uncommon. Fibrous hamartoma of infancy typically occurs in... 
nevus | Congenital | hamartoma | Mole (Dermatology) | Genetic disorders | Hamartoma | Mutation | Pathogenesis | Melanoma | Tumors | Skin cancer | Case Report
Journal Article
AMERICAN JOURNAL OF DERMATOPATHOLOGY, ISSN 0193-1091, 06/2019, Volume 41, Issue 6, pp. 438 - 442
Neurocristic cutaneous hamartomas (NCHs) are rarely reported tumors with divergent differentiation derived from persistently active pluripotent cells from the... 
MELANOCYTIC NEVUS | DISTINCT | congenital nevus | MALIGNANT-MELANOMA | comparative genomic hybridization | proliferative neurocristic hamartoma | BLUE NEVUS | FEATURES | DERMATOLOGY | Case studies | Complications and side effects | Tumors in children | Diagnosis | Mole (Dermatology) | Risk factors | Hamartoma | Skin tumors
Journal Article
RADIOGRAPHICS, ISSN 0271-5333, 07/2019, Volume 39, Issue 4, pp. 1143 - 1160
Although congenital oral masses are rare, they are readily detectable during fetal US screening. Most congenital oral masses are benign, but some may cause... 
MAXILLOFACIAL TUMORS | MANAGEMENT | ANOMALIES | HAMARTOMA | TERATOMA | VASCULAR MALFORMATIONS | HEMANGIOMAS | CYST | CLASSIFICATION | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | PRENATAL-DIAGNOSIS
Journal Article
European Journal of Pediatric Dermatology, ISSN 1122-7672, 10/2016, Volume 26, Issue 4, p. 241
Journal Article
Pediatric Dermatology, ISSN 0736-8046, 07/2015, Volume 32, Issue 4, pp. e167 - e168
A 2‐year‐old girl presented with a congenital, slow‐growing, exophytic nodule on the plantar surface of the foot. Histopathology revealed a hamartoma... 
PEDIATRICS | DERMATOLOGY | Hamartoma - pathology | Diagnosis, Differential | Biopsy | Angiofibroma - pathology | Humans | Child, Preschool | Female | Foot Diseases - pathology | Genetic disorders | Hamartoma
Journal Article
Journal Article
Pediatric Dermatology, ISSN 0736-8046, 07/2017, Volume 34, Issue 4, pp. e216 - e218
Fibroblastic connective tissue nevus (FCTN) is a rare, benign, dermal mesenchymal hamartoma that affects children. We report a 15‐year‐old boy with a... 
PEDIATRICS | DERMAL DENDROCYTE HAMARTOMA | DERMATOLOGY | Diagnosis, Differential | Nevus - diagnosis | Antigens, CD34 - metabolism | Nevus - pathology | Humans | Adolescent | Dermoscopy | Male | Nevus - surgery | Skin - pathology | Mole (Dermatology) | Genetic disorders | Mesenchyme | Microscopy | Benign | Nevus | Skin | Children | Neoplasia
Journal Article
Journal of Cutaneous Pathology, ISSN 0303-6987, 11/2017, Volume 44, Issue 11, pp. 974 - 977
Journal Article
Child's Nervous System, ISSN 0256-7040, 11/2018, Volume 34, Issue 11, pp. 2329 - 2331
Scalp lesions are common pediatric findings that present for neurosurgical evaluation and management. The majority will be benign. Meningothelial hamartomas... 
Scalp mass | Neurosciences | Neurosurgery | Meningothelial hamartoma | Medicine & Public Health | Pediatric | SURGERY | SEBACEUS | PEDIATRICS | CLINICAL NEUROLOGY | Care and treatment | Genetic aspects | Genetic disorders | Diagnosis | Research | Hamartoma
Journal Article
Journal Article
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