Results 161 to 170 of about 111,824 (315)
Near-total jejunoileal atresia with exteriorized cecum and gangrenous appendix associated with gastroschisis: a case report. [PDF]
Yeta DL +3 more
europepmc +1 more source
ABSTRACT Objective This retrospective cohort study aimed to compare the effects of tooth‐bone‐borne mini‐implant‐assisted rapid palatal expansion (MARPE) and tooth‐borne (Hyrax) rapid palatal expansion (RPE) techniques on the pterygopalatine suture (PPS) and the opening pattern of the midpalatal suture (MPS).
Maria Antônia Netto Barbosa +3 more
wiley +1 more source
Management of Azoospermia: A Systematic Approach
ABSTRACT Key Content Work‐up of azoospermic men includes a detailed history, physical examination and investigations to find the underlying cause. Causes and management of azoospermia (pre‐testicular, testicular and post‐testicular) with case presentations.
Naimah Raza +3 more
wiley +1 more source
ABSTRACT Purpose To describe a surgical method for correcting lower lid entropion, lateral canthal entropion, and macroblepharon. Methods Lid margins were incised at a 45° angle, and lateral lid margins and a rhomboid shaped piece of skin were resected based on the degree of macroblepharon.
Maximilian Werner‐Tutschku +1 more
wiley +1 more source
Delayed diagnosis and successful surgical management of bilateral choanal atresia in a 10-year-old male: a case report. [PDF]
Dari MA +4 more
europepmc +1 more source
ABSTRACT Sotos syndrome is an overgrowth disorder caused by nuclear receptor binding SET domain protein 1 (NSD1) haploinsufficiency, whereas reciprocal 5q35.2q35.3 microduplication produces a reversed phenotype with growth retardation, microcephaly, delayed bone age, and neurodevelopmental delay.
Sejin Kim, Jung Sook Ha, Jun Chul Byun
wiley +1 more source
Type-IV intestinal atresia: A challenging congenital anomaly with successful management. [PDF]
Mehdi SR, Liaquat A.
europepmc +1 more source
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken +4 more
wiley +1 more source

