✦ LIBER ✦

Familial DiGeorge syndrome with tetralogy of Fallot and prolonged survival

✍ Scribed by W. E. Winter; J. H. Silverstein; D. J. Barrett; E. Kiel

Publisher: Springer
Year: 1984
Tongue: English
Weight: 242 KB
Volume: 141
Category: Article
ISSN: 0340-6997
DOI: 10.1007/bf00443218

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Familial 22q11.2 deletion: an infant wit

Familial 22q11.2 deletion: an infant with interrupted aortic arch and DiGeorge syndrome delivered from by a mother with tetralogy of Fallot

✍ Tadahiko Ito; Tadashi Okubo; Hiroshi Sato 📂 Article 📅 2002 🏛 Springer 🌐 English ⚖ 55 KB

Teebi hypertelorism syndrome with Tetral

Teebi hypertelorism syndrome with Tetralogy of Fallot

✍ Nakagawa, Masao; Kondo, Masanori; Matsui, Akemi 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 8 KB 👁 3 views

A 34-month-old boy presented with clinical manifestations of Teebi hypertelorism syndrome including prominent forehead with frontal bossing, hypertelorism, exophthalmos due to shallow orbits, a short and broad nose with anteverted nares, small hands and feet with interdigital webbing, umbilical hern

Type III tracheal agenesis with familial

Type III tracheal agenesis with familial tetralogy of Fallot and absent pulmonary value syndrome

✍ Hirt-Armon, Kerri; Pober, Barbara R.; Holmes, Lewis B. 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 366 KB 👁 2 views

We describe a female infant born at 33 weeks gestation diagnosed postnatally with a previously unreported phenotype consisting of Type I11 tracheal agenesis plus tetralogy of Fallot with absent pulmonary valve. She was delivered to a mother who had the same congenital heart malformation, but no dete

A familial disorder with duodenal atresi

A familial disorder with duodenal atresia and tetralogy of Fallot

✍ Lemire, Edmond G.; Evans, Jane A.; Giddins, Niels G.; Harman, Christopher R.; Wi 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 657 KB

We report on two sibs with tetralogy of Fallot (TOF) and duodenal atresia (DA). The first child, a 6-year-old girl, had a right facial palsy in addition to the TOF and DA. Her brother, age 10 months, was born with bilateral microtia without facial palsy. The children are the product of an apparently

Exclusion of 22qll deletion in noonan sy

Exclusion of 22qll deletion in noonan syndrome with tetralogy of fallot

✍ Digilio, Maria Cristina ;Marino, Bruno ;Giannotti, Aldo ;Dallapiccola, Bruno 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 156 KB 👁 3 views

22q11 deletions in isolated and syndromi

22q11 deletions in isolated and syndromic patients with tetralogy of Fallot

✍ Francesca Amati; Aldo Mari; Maria Cristina Digilio; Rita Mingarelli; Bruno Marin 📂 Article 📅 1995 🏛 Springer 🌐 English ⚖ 413 KB