Harper's Textbook of Pediatric Dermatology 2019
DOI: 10.1002/9781119142812.ch135
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Focal Dermal Hypoplasia

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Cited by 23 publications
(66 citation statements)
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References 58 publications
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“…Structural abnormalities of kidneys and urinary system that may lead to recurrent urinary tract infections and urinary reflux may include, hypoplastic kidney, cystic renal dysplasia, hydronephrosis, and fused/horseshoe kidney. [ 12 ] Unilateral agenesis of the kidney with multiple cortical cysts of the contralateral kidney was a notable finding in one of our patients. We could find only one previous report of unilateral absent kidney in PubMed database.…”
Section: Discussionmentioning
confidence: 73%
“…Structural abnormalities of kidneys and urinary system that may lead to recurrent urinary tract infections and urinary reflux may include, hypoplastic kidney, cystic renal dysplasia, hydronephrosis, and fused/horseshoe kidney. [ 12 ] Unilateral agenesis of the kidney with multiple cortical cysts of the contralateral kidney was a notable finding in one of our patients. We could find only one previous report of unilateral absent kidney in PubMed database.…”
Section: Discussionmentioning
confidence: 73%
“…Hair presentations of FDH include patchy alopecia of the scalp (80%) and hair shaft abnormalities on scanning electron microscopy (80–90%). Nail abnormalities of FDH include congenital ridged, dysplastic, or hypoplastic nails (80–90%) [ 11 ]. The cutaneous manifestations of our patient were hypopigmented-reticulated atrophic macules and patches in a linear pattern distributed along the lines of Blaschko over the right side of the face and the right arm.…”
Section: Discussionmentioning
confidence: 99%
“…Skeletal abnormalities of FDH include syndactyly (70–90%), ectrodactyly (75%), long bone reduction defect (50–80%), oligodactyly (20–40%), which more frequently involved central digits, and transverse limb defect (15%) [ 11 ]. In our case, there was not much skeletal involvement.…”
Section: Discussionmentioning
confidence: 99%
“…Kyphoskoliose werden bei ca. 10 % der betroffenen Patienten berichtet, die oft erst im Erwachsenenalter Beschwerden verursachen [9]. Nicht nachweisbar waren bei der Patientin angeborene Malformationen der Extremitäten wie z.…”
Section: Kasuistikunclassified
“…Eine durchschnittlich mildere Ausprägung wird bei den betroffenen Männern durch den Mosaizismus beobachtet, wenngleich auch schwere phänotypische Ausprägungen bei Männern mit einem Mosaizismus der PORCN-Gen-Mutation beschrieben sind [10]. Der Grad der phänotypischen Ausprägung kann durch Mosaizismus oder ungleiche X-Inaktivierung auch bei den betroffenen Frauen stark variieren [9].…”
Section: Diskussionunclassified