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Items: 3

1.

Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies

LTBP4-related cutis laxa is characterized by cutis laxa, early childhood-onset pulmonary emphysema, peripheral pulmonary artery stenosis, and other evidence of a generalized connective tissue disorder such as inguinal hernias and hollow visceral diverticula (e.g., intestine, bladder). Other manifestations can include pyloric stenosis, diaphragmatic hernia, rectal prolapse, gastrointestinal elongation/tortuosity, cardiovascular abnormality, pulmonary hypertension, hypotonia and frequent pulmonary infections. Bladder diverticula and hydronephrosis are common. Early demise has been associated with pulmonary emphysema. [from GeneReviews]

MedGen UID:
442566
Concept ID:
C2750804
Disease or Syndrome
2.

Morgagni diaphragmatic hernia

An anterior retrosternal or parasternal hernia that can result in the herniation of liver or intestines into the chest cavity. [from HPO]

MedGen UID:
539425
Concept ID:
C0265699
Congenital Abnormality
3.

Diamond-Blackfan anemia 10

Diamond-Blackfan anemia (DBA) is characterized by a profound normochromic and usually macrocytic anemia with normal leukocytes and platelets, congenital malformations in up to 50%, and growth deficiency in 30% of affected individuals. The hematologic complications occur in 90% of affected individuals during the first year of life. The phenotypic spectrum ranges from a mild form (e.g., mild anemia or no anemia with only subtle erythroid abnormalities, physical malformations without anemia) to a severe form of fetal anemia resulting in nonimmune hydrops fetalis. DBA is associated with an increased risk for acute myelogenous leukemia (AML), myelodysplastic syndrome (MDS), and solid tumors including osteogenic sarcoma. [from GeneReviews]

MedGen UID:
412873
Concept ID:
C2750080
Disease or Syndrome
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